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MGI:Bcl2

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Bcl2 ( synonyms: Bcl-2 )
Protein Name(s) B cell leukemia/lymphoma 2,
External Links
MGI MGI:88138

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000082

G1/S transition of mitotic cell cycle

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0000082

G1/S transition of mitotic cell cycle

MGI:MGI:3032471
PMID:14660795[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0000082

G1/S transition of mitotic cell cycle

MGI:MGI:3032471
PMID:14660795[2]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0000209

protein polyubiquitination

MGI:MGI:3694309
PMID:16717086[3]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0000902

cell morphogenesis

MGI:MGI:1307011
PMID:10193316[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0001101

response to acid

MGI:MGI:77140
PMID:7675327[5]

IDA: Inferred from Direct Assay

P

From MGI

GO:0001503

ossification

MGI:MGI:1307011
PMID:10193316[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0001541

ovarian follicle development

MGI:MGI:75799
PMID:7628407[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001656

metanephros development

MGI:MGI:70413
PMID:7840250[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001656

metanephros development

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001657

ureteric bud development

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001658

branching involved in ureteric bud morphogenesis

MGI:MGI:3036971
PMID:14699151[9]

IDA: Inferred from Direct Assay

P

From MGI

GO:0001658

branching involved in ureteric bud morphogenesis

MGI:MGI:3768986
PMID:16672320[10]

IGI: Inferred from Genetic Interaction

MGI:MGI:97486

P

From MGI

GO:0001662

behavioral fear response

MGI:MGI:3692132
PMID:16095731[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0001776

leukocyte homeostasis

MGI:MGI:85476
PMID:9028316[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001782

B cell homeostasis

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001782

B cell homeostasis

MGI:MGI:2385423
PMID:7650488[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001822

kidney development

MGI:MGI:1331308
PMID:9950951[15]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001822

kidney development

MGI:MGI:2154874
PMID:11709185[16]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0001822

kidney development

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001822

kidney development

MGI:MGI:3760608
PMID:16282979[17]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001822

kidney development

MGI:MGI:3767491
PMID:15818405[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001822

kidney development

MGI:MGI:3768986
PMID:16672320[10]

IGI: Inferred from Genetic Interaction

MGI:MGI:97486

P

From MGI

GO:0001822

kidney development

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0001822

kidney development

MGI:MGI:70413
PMID:7840250[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001822

kidney development

MGI:MGI:81960
PMID:8760259[20]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0001822

kidney development

MGI:MGI:894988
PMID:9241272[21]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0001952

regulation of cell-matrix adhesion

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0002020

protease binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0002260

lymphocyte homeostasis

MGI:MGI:2154874
PMID:11709185[16]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0002260

lymphocyte homeostasis

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002260

lymphocyte homeostasis

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002260

lymphocyte homeostasis

MGI:MGI:3767491
PMID:15818405[18]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0002320

lymphoid progenitor cell differentiation

MGI:MGI:85476
PMID:9028316[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002326

B cell lineage commitment

MGI:MGI:78866
PMID:8788039[23]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002360

T cell lineage commitment

MGI:MGI:78866
PMID:8788039[23]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002520

immune system development

MGI:MGI:62849
PMID:8372353[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0002520

immune system development

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0003014

renal system process

MGI:MGI:81960
PMID:8760259[20]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0005515

protein binding

MGI:MGI:3527292
PMID:15613488[25]

IPI: Inferred from Physical Interaction

UniProtKB:P11881

F

From MGI

GO:0005515

protein binding

MGI:MGI:3694309
PMID:16717086[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q76MZ3

F

From MGI

GO:0005622

intracellular

MGI:MGI:1928555
PMID:11146504[26]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005622

intracellular

MGI:MGI:85084
PMID:9008714[27]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005622

intracellular

MGI:MGI:894974
PMID:9252127[28]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3702851
PMID:7546744[30]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005634

nucleus

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:67686
PMID:7953633[31]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:69023
PMID:7945396[32]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:71477
PMID:7896880[33]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:3702851
PMID:7546744[30]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P49950

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:74951
PMID:7563251[34]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:77140
PMID:7675327[5]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:2445910
PMID:12420306[35]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:2682130
PMID:14651853[36]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:3852644
PMID:18614015[37]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P49950

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:67686
PMID:7953633[31]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:69023
PMID:7945396[32]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005739

mitochondrion

MGI:MGI:71477
PMID:7896880[33]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005741

mitochondrial outer membrane

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005783

endoplasmic reticulum

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0005783

endoplasmic reticulum

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005789

endoplasmic reticulum membrane

MGI:MGI:3527292
PMID:15613488[25]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005792

microsome

MGI:MGI:67686
PMID:7953633[31]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005792

microsome

MGI:MGI:69023
PMID:7945396[32]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005829

cytosol

MGI:MGI:2385392
PMID:12050152[38]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005829

cytosol

MGI:MGI:2683362
PMID:14551195[39]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005829

cytosol

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0006470

protein dephosphorylation

MGI:MGI:3694309
PMID:16717086[3]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006582

melanin metabolic process

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0006808

regulation of nitrogen utilization

MGI:MGI:894988
PMID:9241272[21]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0006874

cellular calcium ion homeostasis

MGI:MGI:69023
PMID:7945396[32]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006915

apoptotic process

MGI:MGI:67275
PMID:8358790[40]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:1098920
PMID:9374413[41]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:1203837
PMID:9560217[42]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:1330635
PMID:10200548[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:1336407
PMID:10321489[44]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:1350782
PMID:10602483[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:2179928
PMID:12082633[46]

IGI: Inferred from Genetic Interaction

MGI:MGI:1309517

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:2683362
PMID:14551195[39]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:3032471
PMID:14660795[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:3032471
PMID:14660795[2]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:3655321
PMID:9681465[47]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:3700106
PMID:17267035[48]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:3722566
PMID:17068116[49]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P49950

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:49478
PMID:1373874[50]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:64930
PMID:8313913[51]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:68112
PMID:8080725[52]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:68114
PMID:7772249[53]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:68149
PMID:8050499[54]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:70413
PMID:7840250[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:71191
PMID:7751019[55]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:80727
PMID:8663032[56]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:81960
PMID:8760259[20]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:82221
PMID:7834747[57]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:82221
PMID:7834747[57]

IGI: Inferred from Genetic Interaction

MGI:MGI:108047

P

From MGI

GO:0006916

anti-apoptosis

MGI:MGI:894621
PMID:9153592[58]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0006974

response to DNA damage stimulus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0006979

response to oxidative stress

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007015

actin filament organization

MGI:MGI:1331308
PMID:9950951[15]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0007409

axonogenesis

MGI:MGI:85682
PMID:9009190[59]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007569

cell aging

MGI:MGI:62849
PMID:8372353[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0008134

transcription factor binding

MGI:MGI:3721729
PMID:17382917[60]

IPI: Inferred from Physical Interaction

UniProtKB:P10417

F

From MGI

GO:0008219

cell death

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0008219

cell death

MGI:MGI:62849
PMID:8372353[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0008219

cell death

MGI:MGI:67546
PMID:8022822[61]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0008219

cell death

MGI:MGI:84027
PMID:8949945[62]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0008283

cell proliferation

MGI:MGI:1860799
PMID:10762311[63]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0008285

negative regulation of cell proliferation

MGI:MGI:80727
PMID:8663032[56]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0008584

male gonad development

MGI:MGI:894988
PMID:9241272[21]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0009605

response to external stimulus

MGI:MGI:1351727
PMID:10488913[64]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0009636

response to toxin

MGI:MGI:1350782
PMID:10602483[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0009636

response to toxin

MGI:MGI:3694309
PMID:16717086[3]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0009636

response to toxin

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:1352325
PMID:10674380[65]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:2154874
PMID:11709185[16]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:81786
PMID:8755480[66]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:894988
PMID:9241272[21]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0009887

organ morphogenesis

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0010039

response to iron ion

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0010224

response to UV-B

MGI:MGI:1330635
PMID:10200548[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0010332

response to gamma radiation

MGI:MGI:1858868
PMID:10815637[67]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0010332

response to gamma radiation

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0010332

response to gamma radiation

MGI:MGI:3722566
PMID:17068116[49]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0010332

response to gamma radiation

MGI:MGI:62849
PMID:8372353[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0010468

regulation of gene expression

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0010468

regulation of gene expression

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0010523

negative regulation of calcium ion transport into cytosol

MGI:MGI:3527292
PMID:15613488[25]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702
MGI:MGI:1097161
MGI:MGI:96623

P

From MGI

GO:0010559

regulation of glycoprotein biosynthetic process

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0014031

mesenchymal cell development

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0014042

positive regulation of neuron maturation

MGI:MGI:1203785
PMID:9547242[68]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0014911

positive regulation of smooth muscle cell migration

MGI:MGI:3721729
PMID:17382917[60]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0015267

channel activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0016020

membrane

MGI:MGI:71477
PMID:7896880[33]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0016049

cell growth

MGI:MGI:68633
PMID:8084613[69]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0016337

cell-cell adhesion

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0018105

peptidyl-serine phosphorylation

MGI:MGI:3032471
PMID:14660795[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0018107

peptidyl-threonine phosphorylation

MGI:MGI:3032471
PMID:14660795[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0019903

protein phosphatase binding

MGI:MGI:3760740
PMID:12617961[70]

IDA: Inferred from Direct Assay

F

From MGI

GO:0021747

cochlear nucleus development

MGI:MGI:1891561
PMID:11027399[71]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0022612

gland morphogenesis

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0022898

regulation of transmembrane transporter activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0030097

hemopoiesis

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0030183

B cell differentiation

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0030183

B cell differentiation

MGI:MGI:85476
PMID:9028316[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0030217

T cell differentiation

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0030279

negative regulation of ossification

MGI:MGI:85084
PMID:9008714[27]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0030307

positive regulation of cell growth

MGI:MGI:67546
PMID:8022822[61]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0030308

negative regulation of cell growth

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0030318

melanocyte differentiation

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0030318

melanocyte differentiation

MGI:MGI:2180980
PMID:12086670[72]

IGI: Inferred from Genetic Interaction

MGI:MGI:104554

P

From MGI

GO:0030318

melanocyte differentiation

MGI:MGI:2180980
PMID:12086670[72]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0030318

melanocyte differentiation

MGI:MGI:81816
PMID:8758925[73]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0030336

negative regulation of cell migration

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0030890

positive regulation of B cell proliferation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0031103

axon regeneration

MGI:MGI:85682
PMID:9009190[59]

IDA: Inferred from Direct Assay

P

From MGI

GO:0031625

ubiquitin protein ligase binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0031647

regulation of protein stability

MGI:MGI:3032471
PMID:14660795[2]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0031965

nuclear membrane

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0031965

nuclear membrane

MGI:MGI:67308
PMID:8030757[29]

IDA: Inferred from Direct Assay

C

From MGI

GO:0031966

mitochondrial membrane

MGI:MGI:2178871
PMID:11980919[74]

IDA: Inferred from Direct Assay

C

From MGI

GO:0032469

endoplasmic reticulum calcium ion homeostasis

MGI:MGI:3527292
PMID:15613488[25]

IGI: Inferred from Genetic Interaction

MGI:MGI:1097161
MGI:MGI:88138

P

From MGI

GO:0032835

glomerulus development

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0032848

negative regulation of cellular pH reduction

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0032880

regulation of protein localization

MGI:MGI:1331308
PMID:9950951[15]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0033033

negative regulation of myeloid cell apoptotic process

MGI:MGI:892837
PMID:9202146[75]

IDA: Inferred from Direct Assay

P

From MGI

GO:0033077

T cell differentiation in thymus

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0033077

T cell differentiation in thymus

MGI:MGI:85476
PMID:9028316[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0033138

positive regulation of peptidyl-serine phosphorylation

MGI:MGI:3527292
PMID:15613488[25]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702
MGI:MGI:1097161

P

From MGI

GO:0033689

negative regulation of osteoblast proliferation

MGI:MGI:1307011
PMID:10193316[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0034097

response to cytokine stimulus

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0034097

response to cytokine stimulus

MGI:MGI:892164
PMID:9184696[76]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0035094

response to nicotine

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0035265

organ growth

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0035265

organ growth

MGI:MGI:81253
PMID:8623928[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0040007

growth

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0040007

growth

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0040018

positive regulation of multicellular organism growth

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0042100

B cell proliferation

MGI:MGI:49478
PMID:1373874[50]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0042221

response to chemical stimulus

MGI:MGI:77298
PMID:7595537[77]

IDA: Inferred from Direct Assay

P

From MGI

GO:0042493

response to drug

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0042493

response to drug

MGI:MGI:84027
PMID:8949945[62]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0042493

response to drug

MGI:MGI:87440
PMID:9098922[78]

IDA: Inferred from Direct Assay

P

From MGI

GO:0042542

response to hydrogen peroxide

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0042802

identical protein binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0042803

protein homodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0042981

regulation of apoptotic process

MGI:MGI:3767491
PMID:15818405[18]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0043029

T cell homeostasis

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0043029

T cell homeostasis

MGI:MGI:2385423
PMID:7650488[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0043029

T cell homeostasis

MGI:MGI:3760056
PMID:17591857[79]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:2686748
PMID:14707049[80]

IDA: Inferred from Direct Assay

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:3575207
PMID:15776018[81]

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:P10415

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:3584078
PMID:15983387[82]

IDA: Inferred from Direct Assay

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:75819
PMID:7650367[83]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0043067

regulation of programmed cell death

MGI:MGI:3768986
PMID:16672320[10]

IGI: Inferred from Genetic Interaction

MGI:MGI:97486

P

From MGI

GO:0043085

positive regulation of catalytic activity

MGI:MGI:3721729
PMID:17382917[60]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0043209

myelin sheath

MGI:MGI:67686
PMID:7953633[31]

IDA: Inferred from Direct Assay

C

From MGI

GO:0043375

CD8-positive, alpha-beta T cell lineage commitment

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0043496

regulation of protein homodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0043497

regulation of protein heterodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:1860799
PMID:10762311[63]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:1891561
PMID:11027399[71]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:3655321
PMID:9681465[47]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:3702851
PMID:7546744[30]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:77306
PMID:7472523[84]

IDA: Inferred from Direct Assay

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:79659
PMID:8625820[85]

IDA: Inferred from Direct Assay

P

From MGI

GO:0043583

ear development

MGI:MGI:2154874
PMID:11709185[16]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0043583

ear development

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0043583

ear development

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0045636

positive regulation of melanocyte differentiation

MGI:MGI:3618415
PMID:16427619[86]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0045930

negative regulation of mitotic cell cycle

MGI:MGI:894988
PMID:9241272[21]

IDA: Inferred from Direct Assay

P

From MGI

GO:0046671

negative regulation of retinal cell programmed cell death

MGI:MGI:1336407
PMID:10321489[44]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0046930

pore complex

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

C

From MGI

GO:0046982

protein heterodimerization activity

MGI:MGI:1095590
PMID:7834748[87]

IPI: Inferred from Physical Interaction

UniProtKB:Q61337

F

From MGI

GO:0046982

protein heterodimerization activity

MGI:MGI:1347718
PMID:10582606[88]

IPI: Inferred from Physical Interaction

UniProtKB:Q07813

F

From MGI

GO:0046982

protein heterodimerization activity

MGI:MGI:1931634
PMID:11226327[89]

IPI: Inferred from Physical Interaction

UniProtKB:Q07813

F

From MGI

GO:0046982

protein heterodimerization activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P49950

F

From MGI

GO:0046982

protein heterodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0048041

focal adhesion assembly

MGI:MGI:3526739
PMID:15292044[22]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0048066

developmental pigmentation

MGI:MGI:2154874
PMID:11709185[16]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0048066

developmental pigmentation

MGI:MGI:2154874
PMID:11709185[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048066

developmental pigmentation

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048070

regulation of developmental pigmentation

MGI:MGI:3767491
PMID:15818405[18]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0048087

positive regulation of developmental pigmentation

MGI:MGI:1352325
PMID:10674380[65]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0048087

positive regulation of developmental pigmentation

MGI:MGI:894988
PMID:9241272[21]

IGI: Inferred from Genetic Interaction

MGI:MGI:88138

P

From MGI

GO:0048536

spleen development

MGI:MGI:3767491
PMID:15818405[18]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0048536

spleen development

MGI:MGI:3767491
PMID:15818405[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048538

thymus development

MGI:MGI:3767491
PMID:15818405[18]

IGI: Inferred from Genetic Interaction

MGI:MGI:1197519

P

From MGI

GO:0048538

thymus development

MGI:MGI:3767491
PMID:15818405[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048538

thymus development

MGI:MGI:894988
PMID:9241272[21]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0048545

response to steroid hormone stimulus

MGI:MGI:2156164
PMID:8170972[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048546

digestive tract morphogenesis

MGI:MGI:70264
PMID:7812968[19]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0048589

developmental growth

MGI:MGI:3767491
PMID:15818405[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0048599

oocyte development

MGI:MGI:75799
PMID:7628407[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0048743

positive regulation of skeletal muscle fiber development

MGI:MGI:1928555
PMID:11146504[26]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0048753

pigment granule organization

MGI:MGI:81816
PMID:8758925[73]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0048873

homeostasis of number of cells within a tissue

MGI:MGI:3618415
PMID:16427619[86]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2158305

P

From MGI

GO:0048873

homeostasis of number of cells within a tissue

MGI:MGI:894988
PMID:9241272[21]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0050790

regulation of catalytic activity

MGI:MGI:3655321
PMID:9681465[47]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0050853

B cell receptor signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0051384

response to glucocorticoid stimulus

MGI:MGI:62849
PMID:8372353[24]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156165

P

From MGI

GO:0051384

response to glucocorticoid stimulus

MGI:MGI:64930
PMID:8313913[51]

IDA: Inferred from Direct Assay

P

From MGI

GO:0051400

BH domain binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P49950

F

From MGI

GO:0051402

neuron apoptotic process

MGI:MGI:1860799
PMID:10762311[63]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0051402

neuron apoptotic process

MGI:MGI:3702851
PMID:7546744[30]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0051434

BH3 domain binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

F

From MGI

GO:0051607

defense response to virus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0051721

protein phosphatase 2A binding

MGI:MGI:3694309
PMID:16717086[3]

IDA: Inferred from Direct Assay

F

From MGI

GO:0051726

regulation of cell cycle

MGI:MGI:1330635
PMID:10200548[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857430

P

From MGI

GO:0051924

regulation of calcium ion transport

MGI:MGI:67546
PMID:8022822[61]

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI

GO:0070059

apoptosis in response to endoplasmic reticulum stress

MGI:MGI:3575207
PMID:15776018[81]

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:P10415

P

From MGI

GO:0071310

cellular response to organic substance

MGI:MGI:2662654
PMID:12606450[90]

IDA: Inferred from Direct Assay

P

From MGI

GO:0072593

reactive oxygen species metabolic process

MGI:MGI:1354607
PMID:10726970[91]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:0072593

reactive oxygen species metabolic process

MGI:MGI:2679141
PMID:12855558[1]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0072593

reactive oxygen species metabolic process

MGI:MGI:3655321
PMID:9681465[47]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857134

P

From MGI

GO:2001234

negative regulation of apoptotic signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P10415

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Deng X et al. (2003) Bcl2 retards G1/S cell cycle transition by regulating intracellular ROS. Blood 102: 3179-85 PubMed GONUTS page
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Deng X et al. (2004) Mono- and multisite phosphorylation enhances Bcl2's antiapoptotic function and inhibition of cell cycle entry functions. Proc Natl Acad Sci U S A 101: 153-8 PubMed GONUTS page
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Lin SS et al. (2006) PP2A regulates BCL-2 phosphorylation and proteasome-mediated degradation at the endoplasmic reticulum. J Biol Chem 281: 23003-12 PubMed GONUTS page
  4. ↑ 4.0 4.1 4.2 Boot-Handford RP et al. (1998) The bcl-2 knockout mouse exhibits marked changes in osteoblast phenotype and collagen deposition in bone as well as a mild growth plate phenotype. Int J Exp Pathol 79: 329-35 PubMed GONUTS page
  5. ↑ 5.0 5.1 Gillardon F et al. (1995) Up-regulation of bax and down-regulation of bcl-2 is associated with kainate-induced apoptosis in mouse brain. Neurosci Lett 192: 85-8 PubMed GONUTS page
  6. ↑ 6.0 6.1 Ratts VS et al. (1995) Ablation of bcl-2 gene expression decreases the numbers of oocytes and primordial follicles established in the post-natal female mouse gonad. Endocrinology 136: 3665-8 PubMed GONUTS page
  7. ↑ 7.0 7.1 7.2 Sorenson CM et al. (1995) Fulminant metanephric apoptosis and abnormal kidney development in bcl-2-deficient mice. Am J Physiol 268: F73-81 PubMed GONUTS page
  8. ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Nagata M et al. (1996) Apoptosis during an early stage of nephrogenesis induces renal hypoplasia in bcl-2-deficient mice. Am J Pathol 148: 1601-11 PubMed GONUTS page
  9. ↑ Sorenson CM (2004) Interaction of bcl-2 with Paxillin through its BH4 domain is important during ureteric bud branching. J Biol Chem 279: 11368-74 PubMed GONUTS page
  10. ↑ 10.0 10.1 10.2 Dziarmaga A et al. (2006) Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice. J Am Soc Nephrol 17: 1568-75 PubMed GONUTS page
  11. ↑ Einat H et al. (2005) Increased anxiety-like behaviors and mitochondrial dysfunction in mice with targeted mutation of the Bcl-2 gene: further support for the involvement of mitochondrial function in anxiety disorders. Behav Brain Res 165: 172-80 PubMed GONUTS page
  12. ↑ 12.0 12.1 12.2 12.3 Matsuzaki Y et al. (1997) Role of bcl-2 in the development of lymphoid cells from the hematopoietic stem cell. Blood 89: 853-62 PubMed GONUTS page
  13. ↑ 13.00 13.01 13.02 13.03 13.04 13.05 13.06 13.07 13.08 13.09 13.10 13.11 13.12 13.13 13.14 13.15 Nakayama K et al. (1994) Targeted disruption of Bcl-2 alpha beta in mice: occurrence of gray hair, polycystic kidney disease, and lymphocytopenia. Proc Natl Acad Sci U S A 91: 3700-4 PubMed GONUTS page
  14. ↑ 14.0 14.1 Chao DT et al. (1995) Bcl-XL and Bcl-2 repress a common pathway of cell death. J Exp Med 182: 821-8 PubMed GONUTS page
  15. ↑ 15.0 15.1 15.2 Sorenson CM (1999) Nuclear localization of beta-catenin and loss of apical brush border actin in cystic tubules of bcl-2 -/- mice. Am J Physiol 276: F210-7 PubMed GONUTS page
  16. ↑ 16.00 16.01 16.02 16.03 16.04 16.05 16.06 16.07 16.08 16.09 16.10 16.11 16.12 Bouillet P et al. (2001) Degenerative disorders caused by Bcl-2 deficiency prevented by loss of its BH3-only antagonist Bim. Dev Cell 1: 645-53 PubMed GONUTS page
  17. ↑ Hughes P et al. (2006) Loss of PKD1 and loss of Bcl-2 elicit polycystic kidney disease through distinct mechanisms. Cell Death Differ 13: 1123-7 PubMed GONUTS page
  18. ↑ 18.0 18.1 18.2 18.3 18.4 18.5 18.6 18.7 18.8 Bouillet P et al. (2005) Polycystic kidney disease prevented by transgenic RNA interference. Cell Death Differ 12: 831-3 PubMed GONUTS page
  19. ↑ 19.0 19.1 19.2 19.3 19.4 19.5 19.6 19.7 Kamada S et al. (1995) bcl-2 deficiency in mice leads to pleiotropic abnormalities: accelerated lymphoid cell death in thymus and spleen, polycystic kidney, hair hypopigmentation, and distorted small intestine. Cancer Res 55: 354-9 PubMed GONUTS page
  20. ↑ 20.0 20.1 20.2 Sorenson CM et al. (1996) Abnormal postpartum renal development and cystogenesis in the bcl-2 (-/-) mouse. Am J Physiol 271: F184-93 PubMed GONUTS page
  21. ↑ 21.0 21.1 21.2 21.3 21.4 21.5 21.6 21.7 Knudson CM & Korsmeyer SJ (1997) Bcl-2 and Bax function independently to regulate cell death. Nat Genet 16: 358-63 PubMed GONUTS page
  22. ↑ 22.0 22.1 22.2 22.3 22.4 22.5 Ziehr J et al. (2004) Alterations in cell-adhesive and migratory properties of proximal tubule and collecting duct cells from bcl-2 -/- mice. Am J Physiol Renal Physiol 287: F1154-63 PubMed GONUTS page
  23. ↑ 23.0 23.1 Li T et al. (1996) Distinct patterns of Fas cell surface expression during development of T- or B-lymphocyte lineages in normal, scid, and mutant mice lacking or overexpressing p53, bcl-2, or rag-2 genes. Cell Growth Differ 7: 107-14 PubMed GONUTS page
  24. ↑ 24.0 24.1 24.2 24.3 24.4 Nakayama K et al. (1993) Disappearance of the lymphoid system in Bcl-2 homozygous mutant chimeric mice. Science 261: 1584-8 PubMed GONUTS page
  25. ↑ 25.0 25.1 25.2 25.3 25.4 Oakes SA et al. (2005) Proapoptotic BAX and BAK regulate the type 1 inositol trisphosphate receptor and calcium leak from the endoplasmic reticulum. Proc Natl Acad Sci U S A 102: 105-10 PubMed GONUTS page
  26. ↑ 26.0 26.1 Dominov JA et al. (2001) Pro- and anti-apoptotic members of the Bcl-2 family in skeletal muscle: a distinct role for Bcl-2 in later stages of myogenesis. Dev Dyn 220: 18-26 PubMed GONUTS page
  27. ↑ 27.0 27.1 Amling M et al. (1997) Bcl-2 lies downstream of parathyroid hormone-related peptide in a signaling pathway that regulates chondrocyte maturation during skeletal development. J Cell Biol 136: 205-13 PubMed GONUTS page
  28. ↑ von Freeden-Jeffry U et al. (1997) The earliest T lineage-committed cells depend on IL-7 for Bcl-2 expression and normal cell cycle progression. Immunity 7: 147-54 PubMed GONUTS page
  29. ↑ 29.0 29.1 29.2 29.3 29.4 29.5 Novack DV & Korsmeyer SJ (1994) Bcl-2 protein expression during murine development. Am J Pathol 145: 61-73 PubMed GONUTS page
  30. ↑ 30.0 30.1 30.2 30.3 Greenlund LJ et al. (1995) Role of BCL-2 in the survival and function of developing and mature sympathetic neurons. Neuron 15: 649-61 PubMed GONUTS page
  31. ↑ 31.0 31.1 31.2 31.3 Mizuguchi M et al. (1994) Expression of Bcl-2 protein in murine neural cells in culture. Brain Res 649: 197-202 PubMed GONUTS page
  32. ↑ 32.0 32.1 32.2 32.3 Magnelli L et al. (1994) Bcl-2 overexpression abolishes early calcium waving preceding apoptosis in NIH-3T3 murine fibroblasts. Biochem Biophys Res Commun 204: 84-90 PubMed GONUTS page
  33. ↑ 33.0 33.1 33.2 Yang T et al. (1995) The intracellular distribution and pattern of expression of Mcl-1 overlap with, but are not identical to, those of Bcl-2. J Cell Biol 128: 1173-84 PubMed GONUTS page
  34. ↑ Gillardon F et al. (1995) Differential regulation of bcl-2, bax, c-fos, junB, and krox-24 expression in the cerebellum of Purkinje cell degeneration mutant mice. J Neurosci Res 41: 708-15 PubMed GONUTS page
  35. ↑ Nakamura N et al. (2003) Sorting specificity of spermatogenic cell specific region of mouse hexokinase-s (mHk1-s). Mol Reprod Dev 64: 113-9 PubMed GONUTS page
  36. ↑ Mootha VK et al. (2003) Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria. Cell 115: 629-40 PubMed GONUTS page
  37. ↑ Pagliarini DJ et al. (2008) A mitochondrial protein compendium elucidates complex I disease biology. Cell 134: 112-23 PubMed GONUTS page
  38. ↑ Hu J et al. (2002) A novel transactivating factor that regulates interferon-gamma-dependent gene expression. J Biol Chem 277: 30253-63 PubMed GONUTS page
  39. ↑ 39.0 39.1 Kocher O et al. (2003) Targeted disruption of the PDZK1 gene in mice causes tissue-specific depletion of the high density lipoprotein receptor scavenger receptor class B type I and altered lipoprotein metabolism. J Biol Chem 278: 52820-5 PubMed GONUTS page
  40. ↑ Oltvai ZN et al. (1993) Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell 74: 609-19 PubMed GONUTS page
  41. ↑ Piñón LG et al. (1997) Bcl-2 is required for cranial sensory neuron survival at defined stages of embryonic development. Development 124: 4173-8 PubMed GONUTS page
  42. ↑ Jürgensmeier JM et al. (1998) Bax directly induces release of cytochrome c from isolated mitochondria. Proc Natl Acad Sci U S A 95: 4997-5002 PubMed GONUTS page
  43. ↑ 43.0 43.1 43.2 Gillardon F et al. (1999) Alterations in cell death and cell cycle progression in the UV-irradiated epidermis of bcl-2-deficient mice. Cell Death Differ 6: 55-60 PubMed GONUTS page
  44. ↑ 44.0 44.1 Cellerino A et al. (1999) Retinal ganglion cell loss after the period of naturally occurring cell death in bcl-2-/- mice. Neuroreport 10: 1091-5 PubMed GONUTS page
  45. ↑ 45.0 45.1 Pritchard DM et al. (1999) Damage-induced apoptosis in intestinal epithelia from bcl-2-null and bax-null mice: investigations of the mechanistic determinants of epithelial apoptosis in vivo. Oncogene 18: 7287-93 PubMed GONUTS page
  46. ↑ Fleischer A et al. (2002) Proapoptotic activity of ITM2B(s), a BH3-only protein induced upon IL-2-deprivation which interacts with Bcl-2. Oncogene 21: 3181-9 PubMed GONUTS page
  47. ↑ 47.0 47.1 47.2 47.3 Hochman A et al. (1998) Enhanced oxidative stress and altered antioxidants in brains of Bcl-2-deficient mice. J Neurochem 71: 741-8 PubMed GONUTS page
  48. ↑ Chen M et al. (2007) Regulation of the lifespan in dendritic cell subsets. Mol Immunol 44: 2558-65 PubMed GONUTS page
  49. ↑ 49.0 49.1 Przemeck SM et al. (2007) Radiation-induced gastric epithelial apoptosis occurs in the proliferative zone and is regulated by p53, bak, bax, and bcl-2. Am J Physiol Gastrointest Liver Physiol 292: G620-7 PubMed GONUTS page
  50. ↑ 50.0 50.1 Borzillo GV et al. (1992) Bcl-2 confers growth and survival advantage to interleukin 7-dependent early pre-B cells which become factor independent by a multistep process in culture. Oncogene 7: 869-76 PubMed GONUTS page
  51. ↑ 51.0 51.1 Merino R et al. (1994) Developmental regulation of the Bcl-2 protein and susceptibility to cell death in B lymphocytes. EMBO J 13: 683-91 PubMed GONUTS page
  52. ↑ Kondo S et al. (1994) bcl-2 gene enables rescue from in vitro myelosuppression (bone marrow cell death) induced by chemotherapy. Br J Cancer 70: 421-6 PubMed GONUTS page
  53. ↑ Takayama S et al. (1994) Evolutionary conservation of function among mammalian, avian, and viral homologs of the Bcl-2 oncoprotein. DNA Cell Biol 13: 679-92 PubMed GONUTS page
  54. ↑ Kondo S et al. (1994) bcl-2 gene prevents apoptosis of basic fibroblast growth factor-deprived murine aortic endothelial cells. Exp Cell Res 213: 428-32 PubMed GONUTS page
  55. ↑ Broome HE et al. (1995) Apoptosis and Bcl-2 expression in cultured murine splenic T cells. Immunology 84: 375-82 PubMed GONUTS page
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  57. ↑ 57.0 57.1 Takayama S et al. (1995) Cloning and functional analysis of BAG-1: a novel Bcl-2-binding protein with anti-cell death activity. Cell 80: 279-84 PubMed GONUTS page
  58. ↑ Tanabe H et al. (1997) Susceptibility of cerebellar granule neurons derived from Bcl-2-deficient and transgenic mice to cell death. Eur J Neurosci 9: 848-56 PubMed GONUTS page
  59. ↑ 59.0 59.1 Chen DF et al. (1997) Bcl-2 promotes regeneration of severed axons in mammalian CNS. Nature 385: 434-9 PubMed GONUTS page
  60. ↑ 60.0 60.1 60.2 Hou Y et al. (2007) c-Myc is essential for urokinase plasminogen activator expression on hypoxia-induced vascular smooth muscle cells. Cardiovasc Res 75: 186-94 PubMed GONUTS page
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  62. ↑ 62.0 62.1 Lezoualc'h F et al. (1996) Bcl-2 prevents hippocampal cell death induced by the neuroleptic drug haloperidol. Brain Res 738: 176-9 PubMed GONUTS page
  63. ↑ 63.0 63.1 63.2 Middleton G et al. (2000) Differences in bcl-2- and bax-independent function in regulating apoptosis in sensory neuron populations. Eur J Neurosci 12: 819-27 PubMed GONUTS page
  64. ↑ Hata R et al. (1999) Targeted disruption of the bcl-2 gene in mice exacerbates focal ischemic brain injury. Metab Brain Dis 14: 117-24 PubMed GONUTS page
  65. ↑ 65.0 65.1 Müller-Röver S et al. (1999) Hair follicle apoptosis and Bcl-2. J Investig Dermatol Symp Proc 4: 272-7 PubMed GONUTS page
  66. ↑ Michaelidis TM et al. (1996) Inactivation of bcl-2 results in progressive degeneration of motoneurons, sympathetic and sensory neurons during early postnatal development. Neuron 17: 75-89 PubMed GONUTS page
  67. ↑ Hendry JH et al. (2000) Effects of deficiency in p53 or bcl-2 on the sensitivity of clonogenic cells in the small intestine to low dose-rate irradiation. Int J Radiat Biol 76: 559-65 PubMed GONUTS page
  68. ↑ Middleton G et al. (1998) Bcl-2 accelerates the maturation of early sensory neurons. J Neurosci 18: 3344-50 PubMed GONUTS page
  69. ↑ Cotter FE et al. (1994) Antisense oligonucleotides suppress B-cell lymphoma growth in a SCID-hu mouse model. Oncogene 9: 3049-55 PubMed GONUTS page
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  72. ↑ 72.0 72.1 McGill GG et al. (2002) Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability. Cell 109: 707-18 PubMed GONUTS page
  73. ↑ 73.0 73.1 Yamamura K et al. (1996) Accelerated disappearance of melanocytes in bcl-2-deficient mice. Cancer Res 56: 3546-50 PubMed GONUTS page
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  75. ↑ Barge RM et al. (1997) Differential involvement of caspases in apoptosis of myeloid leukemic cells induced by chemotherapy versus growth factor withdrawal. FEBS Lett 409: 207-10 PubMed GONUTS page
  76. ↑ Li L et al. (1997) The apoptosis and proliferation of SAC-activated B cells by IL-10 are associated with changes in Bcl-2, Bcl-xL, and Mcl-1 expression. Cell Immunol 178: 33-41 PubMed GONUTS page
  77. ↑ Myers KM et al. (1995) Bcl-2 protects neural cells from cyanide/aglycemia-induced lipid oxidation, mitochondrial injury, and loss of viability. J Neurochem 65: 2432-40 PubMed GONUTS page
  78. ↑ Wlodarczyk BC et al. (1996) Valproic acid-induced changes in gene expression during neurulation in a mouse model. Teratology 54: 284-97 PubMed GONUTS page
  79. ↑ Wojciechowski S et al. (2007) Bim/Bcl-2 balance is critical for maintaining naive and memory T cell homeostasis. J Exp Med 204: 1665-75 PubMed GONUTS page
  80. ↑ Jung KC et al. (2004) TCR-independent and caspase-independent apoptosis of murine thymocytes by CD24 cross-linking. J Immunol 172: 795-802 PubMed GONUTS page
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  82. ↑ Ishii H et al. (2005) Frag1, a homolog of alternative replication factor C subunits, links replication stress surveillance with apoptosis. Proc Natl Acad Sci U S A 102: 9655-60 PubMed GONUTS page
  83. ↑ Broome HE et al. (1995) Expression of Bcl-2, Bcl-x, and Bax after T cell activation and IL-2 withdrawal. J Immunol 155: 2311-7 PubMed GONUTS page
  84. ↑ Sagot Y et al. (1995) Bcl-2 overexpression prevents motoneuron cell body loss but not axonal degeneration in a mouse model of a neurodegenerative disease. J Neurosci 15: 7727-33 PubMed GONUTS page
  85. ↑ Middleton G et al. (1996) Bax promotes neuronal survival and antagonises the survival effects of neurotrophic factors. Development 122: 695-701 PubMed GONUTS page
  86. ↑ 86.0 86.1 Mak SS et al. (2006) Indispensable role of Bcl2 in the development of the melanocyte stem cell. Dev Biol 291: 144-53 PubMed GONUTS page
  87. ↑ Yang E et al. (1995) Bad, a heterodimeric partner for Bcl-XL and Bcl-2, displaces Bax and promotes cell death. Cell 80: 285-91 PubMed GONUTS page
  88. ↑ Vukosavic S et al. (1999) Bax and Bcl-2 interaction in a transgenic mouse model of familial amyotrophic lateral sclerosis. J Neurochem 73: 2460-8 PubMed GONUTS page
  89. ↑ Vila M et al. (2001) Bax ablation prevents dopaminergic neurodegeneration in the 1-methyl- 4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson's disease. Proc Natl Acad Sci U S A 98: 2837-42 PubMed GONUTS page
  90. ↑ Mu J et al. (2003) Apoptosis and related proteins in placenta of intrauterine fetal death in prostaglandin f receptor-deficient mice. Biol Reprod 68: 1968-74 PubMed GONUTS page
  91. ↑ Hochman A et al. (2000) Developmental changes in antioxidant enzymes and oxidative damage in kidneys, liver and brain of bcl-2 knockout mice. Cell Mol Biol (Noisy-le-grand) 46: 41-52 PubMed GONUTS page
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