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MGI:Cited2

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Cited2 ( synonyms: Mrg1, Msg2, p35srj )
Protein Name(s) Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2,
External Links
MGI MGI:1306784

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000122

negative regulation of transcription from RNA polymerase II promoter

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0001102

RNA polymerase II activating transcription factor binding

MGI:MGI:2179743
PMID:11694877[1]

IPI: Inferred from Physical Interaction

UniProtKB:P34056
UniProtKB:Q61313
UniProtKB:Q61312

F

From MGI

GO:0001105

RNA polymerase II transcription coactivator activity

MGI:MGI:2179743
PMID:11694877[1]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001105

RNA polymerase II transcription coactivator activity

MGI:MGI:3690196
PMID:16619037[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001568

blood vessel development

MGI:MGI:3606737
PMID:15615595[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0001570

vasculogenesis

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0001666

response to hypoxia

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0001701

in utero embryonic development

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0001829

trophectodermal cell differentiation

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0001841

neural tube formation

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0001843

neural tube closure

MGI:MGI:2384266
PMID:12149478[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0001889

liver development

MGI:MGI:3847632
PMID:17644732[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0001892

embryonic placenta development

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0001944

vasculature development

MGI:MGI:3807101
PMID:18653562[7]

IGI: Inferred from Genetic Interaction

MGI:MGI:106918

P

From MGI

GO:0001944

vasculature development

MGI:MGI:3807101
PMID:18653562[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0001947

heart looping

MGI:MGI:3574743
PMID:15750185[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0002089

lens morphogenesis in camera-type eye

MGI:MGI:3807101
PMID:18653562[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3696062
MGI:MGI:3045749

P

From MGI

GO:0002244

hemopoietic progenitor cell differentiation

MGI:MGI:3847632
PMID:17644732[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0002521

leukocyte differentiation

MGI:MGI:3847632
PMID:17644732[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0003151

outflow tract morphogenesis

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0003197

endocardial cushion development

MGI:MGI:3574743
PMID:15750185[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0003281

ventricular septum development

MGI:MGI:2384266
PMID:12149478[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0003281

ventricular septum development

MGI:MGI:3574743
PMID:15750185[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0003682

chromatin binding

MGI:MGI:3690196
PMID:16619037[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003682

chromatin binding

MGI:MGI:3807101
PMID:18653562[7]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003712

transcription cofactor activity

MGI:MGI:2159043
PMID:11823447[9]

TAS: Traceable Author Statement

F

From MGI

GO:0003713

transcription coactivator activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

F

From MGI

GO:0003714

transcription corepressor activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

F

From MGI

GO:0005634

nucleus

MGI:MGI:3807101
PMID:18653562[7]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

C

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:2159043
PMID:11823447[9]

TAS: Traceable Author Statement

P

From MGI

GO:0006357

regulation of transcription from RNA polymerase II promoter

MGI:MGI:3054669
PMID:15475956[10]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007179

transforming growth factor beta receptor signaling pathway

MGI:MGI:3690196
PMID:16619037[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007417

central nervous system development

MGI:MGI:2159043
PMID:11823447[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0007422

peripheral nervous system development

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0007507

heart development

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0008283

cell proliferation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0008584

male gonad development

MGI:MGI:3851651
PMID:19457926[11]

IGI: Inferred from Genetic Interaction

MGI:MGI:1346833

P

From MGI

GO:0008584

male gonad development

MGI:MGI:3851651
PMID:19457926[11]

IGI: Inferred from Genetic Interaction

MGI:MGI:98968

P

From MGI

GO:0010628

positive regulation of gene expression

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0010629

negative regulation of gene expression

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0021602

cranial nerve morphogenesis

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0030325

adrenal gland development

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0030325

adrenal gland development

MGI:MGI:3606737
PMID:15615595[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0030336

negative regulation of cell migration

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0030851

granulocyte differentiation

MGI:MGI:3847632
PMID:17644732[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0034405

response to fluid shear stress

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0035360

positive regulation of peroxisome proliferator activated receptor signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0043627

response to estrogen stimulus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0045892

negative regulation of transcription, DNA-dependent

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0045893

positive regulation of transcription, DNA-dependent

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

P

From MGI

GO:0046332

SMAD binding

MGI:MGI:3690196
PMID:16619037[2]

IPI: Inferred from Physical Interaction

UniProtKB:Q62432
UniProtKB:Q8BUN5

F

From MGI

GO:0046697

decidualization

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0048538

thymus development

MGI:MGI:4457799
PMID:20549734[12]

IGI: Inferred from Genetic Interaction

MGI:MGI:109360

P

From MGI

GO:0048538

thymus development

MGI:MGI:4457799
PMID:20549734[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0048596

embryonic camera-type eye morphogenesis

MGI:MGI:3807101
PMID:18653562[7]

IGI: Inferred from Genetic Interaction

MGI:MGI:97490

P

From MGI

GO:0048821

erythrocyte development

MGI:MGI:3847632
PMID:17644732[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0050693

LBD domain binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q99967

F

From MGI

GO:0060136

embryonic process involved in female pregnancy

MGI:MGI:3628724
PMID:16579983[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

P

From MGI

GO:0060349

bone morphogenesis

MGI:MGI:4457799
PMID:20549734[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0060411

cardiac septum morphogenesis

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0061156

pulmonary artery morphogenesis

MGI:MGI:2384266
PMID:12149478[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2385355

P

From MGI

GO:0061308

cardiac neural crest cell development involved in heart development

MGI:MGI:2179743
PMID:11694877[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2179740

P

From MGI

GO:0061371

determination of heart left/right asymmetry

MGI:MGI:3574743
PMID:15750185[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2176158

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 Bamforth SD et al. (2001) Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator. Nat Genet 29: 469-74 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 Chou YT et al. (2006) Cited2 modulates TGF-beta-mediated upregulation of MMP9. Oncogene 25: 5547-60 PubMed GONUTS page
  3. 3.0 3.1 Schneider JE et al. (2004) Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique. BMC Dev Biol 4: 16 PubMed GONUTS page
  4. 4.0 4.1 4.2 4.3 4.4 4.5 Withington SL et al. (2006) Loss of Cited2 affects trophoblast formation and vascularization of the mouse placenta. Dev Biol 294: 67-82 PubMed GONUTS page
  5. 5.0 5.1 5.2 Yin Z et al. (2002) The essential role of Cited2, a negative regulator for HIF-1alpha, in heart development and neurulation. Proc Natl Acad Sci U S A 99: 10488-93 PubMed GONUTS page
  6. 6.0 6.1 6.2 6.3 6.4 Chen Y et al. (2007) Cited2 is required for normal hematopoiesis in the murine fetal liver. Blood 110: 2889-98 PubMed GONUTS page
  7. 7.0 7.1 7.2 7.3 7.4 7.5 Chen Y et al. (2008) Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis. Development 135: 2939-48 PubMed GONUTS page
  8. 8.0 8.1 8.2 8.3 Weninger WJ et al. (2005) Cited2 is required both for heart morphogenesis and establishment of the left-right axis in mouse development. Development 132: 1337-48 PubMed GONUTS page
  9. 9.0 9.1 9.2 Barbera JP et al. (2002) Folic acid prevents exencephaly in Cited2 deficient mice. Hum Mol Genet 11: 283-93 PubMed GONUTS page
  10. Bamforth SD et al. (2004) Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway. Nat Genet 36: 1189-96 PubMed GONUTS page
  11. 11.0 11.1 Buaas FW et al. (2009) The transcription co-factor CITED2 functions during sex determination and early gonad development. Hum Mol Genet 18: 2989-3001 PubMed GONUTS page
  12. 12.0 12.1 12.2 Michell AC et al. (2010) A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2. Dev Dyn 239: 1988-94 PubMed GONUTS page
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