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MGI:Atg7

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Atg7 ( synonyms: Apg7l )
Protein Name(s) autophagy-related 7 (yeast),
External Links
MGI MGI:1921494

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000166

nucleotide binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR016040

F

From MGI

GO:0001889

liver development

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176073

P

From MGI

GO:0003824

catalytic activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000594

F

From MGI

GO:0004839

ubiquitin activating enzyme activity

MGI:MGI:2177369
PMID:11890701[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005515

protein binding

MGI:MGI:2177369
PMID:11890701[2]

IPI: Inferred from Physical Interaction

UniProtKB:Q9CQY1
UniProtKB:Q9DCD6
UniProtKB:Q9CQV6
UniProtKB:Q9DCD8

F

From MGI

GO:0005515

protein binding

MGI:MGI:2447271
PMID:12482611[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q8R1P4
UniProtKB:Q9CQY1

F

From MGI

GO:0005737

cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:C9JFF4

C

From MGI

GO:0006497

protein lipidation

MGI:MGI:2677578
PMID:12890687[4]

ISO: Inferred from Sequence Orthology

UniProtKB:O95352

P

From MGI

GO:0006520

cellular amino acid metabolic process

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176052

P

From MGI

GO:0006810

transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0813

P

From MGI

GO:0006914

autophagy

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176052

P

From MGI

GO:0006914

autophagy

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176073

P

From MGI

GO:0006914

autophagy

MGI:MGI:3653078
PMID:16885219[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587771

P

From MGI

GO:0006914

autophagy

MGI:MGI:3711608
PMID:17450150[6]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0006914

autophagy

MGI:MGI:3722981
PMID:17726112[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2137515

P

From MGI

GO:0006914

autophagy

MGI:MGI:4829568
PMID:20577052[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769

P

From MGI

GO:0006996

organelle organization

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176073

P

From MGI

GO:0007628

adult walking behavior

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176052

P

From MGI

GO:0009791

post-embryonic development

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0015031

protein transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0653

P

From MGI

GO:0016044

cellular membrane organization

MGI:MGI:3722981
PMID:17726112[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2137515

P

From MGI

GO:0019778

APG12 activating enzyme activity

MGI:MGI:4835103
PMID:20723759[10]

IMP: Inferred from Mutant Phenotype

F

From MGI

GO:0021680

cerebellar Purkinje cell layer development

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0021680

cerebellar Purkinje cell layer development

MGI:MGI:4829568
PMID:20577052[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769

P

From MGI

GO:0021860

pyramidal neuron development

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0021955

central nervous system neuron axonogenesis

MGI:MGI:4829568
PMID:20577052[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769

P

From MGI

GO:0021987

cerebral cortex development

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0030163

protein catabolic process

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176073

P

From MGI

GO:0031175

neuron projection development

MGI:MGI:3722981
PMID:17726112[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2137515

P

From MGI

GO:0031396

regulation of protein ubiquitination

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0031401

positive regulation of protein modification process

MGI:MGI:2447271
PMID:12482611[3]

IDA: Inferred from Direct Assay

P

From MGI

GO:0031401

positive regulation of protein modification process

MGI:MGI:2677578
PMID:12890687[4]

ISO: Inferred from Sequence Orthology

UniProtKB:O95352

P

From MGI

GO:0032446

protein modification by small protein conjugation

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176052

P

From MGI

GO:0042594

response to starvation

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176052

P

From MGI

GO:0042594

response to starvation

MGI:MGI:3587473
PMID:15866887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2176073

P

From MGI

GO:0042803

protein homodimerization activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:O95352

F

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0043066

negative regulation of apoptotic process

MGI:MGI:3711608
PMID:17450150[6]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0050877

neurological system process

MGI:MGI:3630371
PMID:16625205[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3587769
MGI:MGI:2386545

P

From MGI

GO:0055013

cardiac muscle cell development

MGI:MGI:3711608
PMID:17450150[6]

IMP: Inferred from Mutant Phenotype

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 1.8 1.9 Komatsu M et al. (2005) Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice. J Cell Biol 169: 425-34 PubMed GONUTS page
  2. 2.0 2.1 Tanida I et al. (2002) Murine Apg12p has a substrate preference for murine Apg7p over three Apg8p homologs. Biochem Biophys Res Commun 292: 256-62 PubMed GONUTS page
  3. 3.0 3.1 Mizushima N et al. (2002) Mouse Apg10 as an Apg12-conjugating enzyme: analysis by the conjugation-mediated yeast two-hybrid method. FEBS Lett 532: 450-4 PubMed GONUTS page
  4. 4.0 4.1 Nemoto T et al. (2003) The mouse APG10 homologue, an E2-like enzyme for Apg12p conjugation, facilitates MAP-LC3 modification. J Biol Chem 278: 39517-26 PubMed GONUTS page
  5. Wang QJ et al. (2006) Induction of autophagy in axonal dystrophy and degeneration. J Neurosci 26: 8057-68 PubMed GONUTS page
  6. 6.0 6.1 6.2 Nakai A et al. (2007) The role of autophagy in cardiomyocytes in the basal state and in response to hemodynamic stress. Nat Med 13: 619-24 PubMed GONUTS page
  7. 7.0 7.1 7.2 Komatsu M et al. (2007) Essential role for autophagy protein Atg7 in the maintenance of axonal homeostasis and the prevention of axonal degeneration. Proc Natl Acad Sci U S A 104: 14489-94 PubMed GONUTS page
  8. 8.0 8.1 8.2 Mariño G et al. (2010) Autophagy is essential for mouse sense of balance. J Clin Invest 120: 2331-44 PubMed GONUTS page
  9. 9.0 9.1 9.2 9.3 9.4 9.5 9.6 9.7 Komatsu M et al. (2006) Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature 441: 880-4 PubMed GONUTS page
  10. Radoshevich L et al. (2010) ATG12 conjugation to ATG3 regulates mitochondrial homeostasis and cell death. Cell 142: 590-600 PubMed GONUTS page
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