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MGI:Nanog

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Nanog ( synonyms: ecat4, ENK )
Protein Name(s) Nanog homeobox,
External Links
MGI MGI:1919200

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:3654744
PMID:16801560[1]

IGI: Inferred from Genetic Interaction

MGI:MGI:103302
MGI:MGI:1276116

P

From MGI

GO:0001158

enhancer sequence-specific DNA binding

MGI:MGI:4946171
PMID:21062744[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001710

mesodermal cell fate commitment

MGI:MGI:3654744
PMID:16801560[1]

IGI: Inferred from Genetic Interaction

MGI:MGI:109452

P

From MGI

GO:0001714

endodermal cell fate specification

MGI:MGI:4887279
PMID:21245162[3]

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0003677

DNA binding

MGI:MGI:2661864
PMID:12787504[4]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003677

DNA binding

MGI:MGI:3621412
PMID:16518401[5]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003677

DNA binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

F

From MGI

GO:0003682

chromatin binding

MGI:MGI:3804326
PMID:18467660[6]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003700

sequence-specific DNA binding transcription factor activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

F

From MGI

GO:0005515

protein binding

MGI:MGI:4399017
PMID:17093407[7]

IPI: Inferred from Physical Interaction

UniProtKB:P20263
UniProtKB:P70414
UniProtKB:Q4FK52
UniProtKB:Q61066
UniProtKB:Q6PR54

F

From MGI

GO:0005515

protein binding

MGI:MGI:4946164
PMID:21076177[8]

IPI: Inferred from Physical Interaction

UniProtKB:Q5BL09

F

From MGI

GO:0005515

protein binding

MGI:MGI:4946171
PMID:21062744[2]

IPI: Inferred from Physical Interaction

UniProtKB:Q9ER74

F

From MGI

GO:0005625

soluble fraction

MGI:MGI:4367296
PMID:19796622[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3527362
PMID:15582778[10]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3578587
PMID:15788452[11]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3608143
PMID:16259959[12]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3799386
PMID:18425773[13]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4367296
PMID:19796622[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_001094251

C

From MGI

GO:0005634

nucleus

MGI:MGI:4422111
PMID:20123909[14]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4889168
PMID:20937355[15]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4946462
PMID:21146513[16]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005654

nucleoplasm

MGI:MGI:4946164
PMID:21076177[8]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005730

nucleolus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

C

From MGI

GO:0006351

transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0804

P

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0007275

multicellular organismal development

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0217

P

From MGI

GO:0008283

cell proliferation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0008284

positive regulation of cell proliferation

MGI:MGI:3608143
PMID:16259959[12]

IDA: Inferred from Direct Assay

P

From MGI

GO:0009790

embryo development

MGI:MGI:2661864
PMID:12787504[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2664492

P

From MGI

GO:0010454

negative regulation of cell fate commitment

MGI:MGI:3654744
PMID:16801560[1]

IDA: Inferred from Direct Assay

P

From MGI

GO:0010454

negative regulation of cell fate commitment

MGI:MGI:3654744
PMID:16801560[1]

IGI: Inferred from Genetic Interaction

MGI:MGI:109452

P

From MGI

GO:0010468

regulation of gene expression

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0017145

stem cell division

MGI:MGI:2663314
PMID:12787505[17]

IDA: Inferred from Direct Assay

P

From MGI

GO:0019827

stem cell maintenance

MGI:MGI:2661864
PMID:12787504[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2664492

P

From MGI

GO:0019827

stem cell maintenance

MGI:MGI:3654397
PMID:16767105[18]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0019827

stem cell maintenance

MGI:MGI:3654744
PMID:16801560[1]

IDA: Inferred from Direct Assay

P

From MGI

GO:0030514

negative regulation of BMP signaling pathway

MGI:MGI:3654744
PMID:16801560[1]

IDA: Inferred from Direct Assay

P

From MGI

GO:0032526

response to retinoic acid

MGI:MGI:3795829
PMID:18400104[19]

IDA: Inferred from Direct Assay

P

From MGI

GO:0035019

somatic stem cell maintenance

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0042221

response to chemical stimulus

MGI:MGI:3795829
PMID:18400104[19]

IDA: Inferred from Direct Assay

P

From MGI

GO:0042664

negative regulation of endodermal cell fate specification

MGI:MGI:3690198
PMID:16501172[20]

TAS: Traceable Author Statement

P

From MGI

GO:0043565

sequence-specific DNA binding

MGI:MGI:3795829
PMID:18400104[19]

IDA: Inferred from Direct Assay

F

From MGI

GO:0043565

sequence-specific DNA binding

MGI:MGI:4889168
PMID:20937355[15]

IDA: Inferred from Direct Assay

F

From MGI

GO:0044212

transcription regulatory region DNA binding

MGI:MGI:4422111
PMID:20123909[14]

IDA: Inferred from Direct Assay

F

From MGI

GO:0045595

regulation of cell differentiation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0045596

negative regulation of cell differentiation

MGI:MGI:3764939
PMID:17940068[21]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045596

negative regulation of cell differentiation

MGI:MGI:3764939
PMID:17940068[21]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045893

positive regulation of transcription, DNA-dependent

MGI:MGI:4889168
PMID:20937355[15]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0045931

positive regulation of mitotic cell cycle

MGI:MGI:3608143
PMID:16259959[12]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:4887279
PMID:21245162[3]

ISO: Inferred from Sequence Orthology

UniProtKB:Q9H9S0

P

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:4889168
PMID:20937355[15]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0048863

stem cell differentiation

MGI:MGI:3689688
PMID:16894029[22]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0048863

stem cell differentiation

MGI:MGI:4422111
PMID:20123909[14]

IDA: Inferred from Direct Assay

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 Suzuki A et al. (2006) Nanog binds to Smad1 and blocks bone morphogenetic protein-induced differentiation of embryonic stem cells. Proc Natl Acad Sci U S A 103: 10294-9 PubMed GONUTS page
  2. 2.0 2.1 Karantzali E et al. (2011) Sall1 regulates embryonic stem cell differentiation in association with nanog. J Biol Chem 286: 1037-45 PubMed GONUTS page
  3. 3.0 3.1 Teo AK et al. (2011) Pluripotency factors regulate definitive endoderm specification through eomesodermin. Genes Dev 25: 238-50 PubMed GONUTS page
  4. 4.0 4.1 4.2 Mitsui K et al. (2003) The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells. Cell 113: 631-42 PubMed GONUTS page
  5. Loh YH et al. (2006) The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells. Nat Genet 38: 431-40 PubMed GONUTS page
  6. Tam WL et al. (2008) T-cell factor 3 regulates embryonic stem cell pluripotency and self-renewal by the transcriptional control of multiple lineage pathways. Stem Cells 26: 2019-31 PubMed GONUTS page
  7. Wang J et al. (2006) A protein interaction network for pluripotency of embryonic stem cells. Nature 444: 364-8 PubMed GONUTS page
  8. 8.0 8.1 Johansson H & Simonsson S (2010) Core transcription factors, Oct4, Sox2 and Nanog, individually form complexes with nucleophosmin (Npm1) to control embryonic stem (ES) cell fate determination. Aging (Albany NY) 2: 815-22 PubMed GONUTS page
  9. 9.0 9.1 Nishiyama A et al. (2009) Uncovering early response of gene regulatory networks in ESCs by systematic induction of transcription factors. Cell Stem Cell 5: 420-33 PubMed GONUTS page
  10. Hatano SY et al. (2005) Pluripotential competence of cells associated with Nanog activity. Mech Dev 122: 67-79 PubMed GONUTS page
  11. Strumpf D et al. (2005) Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst. Development 132: 2093-102 PubMed GONUTS page
  12. 12.0 12.1 12.2 Zhang J et al. (2005) Expression of Nanog gene promotes NIH3T3 cell proliferation. Biochem Biophys Res Commun 338: 1098-102 PubMed GONUTS page
  13. Strizzi L et al. (2008) Netrin-1 can affect morphogenesis and differentiation of the mouse mammary gland. J Cell Physiol 216: 824-34 PubMed GONUTS page
  14. 14.0 14.1 14.2 Niakan KK et al. (2010) Sox17 promotes differentiation in mouse embryonic stem cells by directly regulating extraembryonic gene expression and indirectly antagonizing self-renewal. Genes Dev 24: 312-26 PubMed GONUTS page
  15. 15.0 15.1 15.2 15.3 Kelly VR & Hammer GD (2011) LRH-1 and Nanog regulate Dax1 transcription in mouse embryonic stem cells. Mol Cell Endocrinol 332: 116-24 PubMed GONUTS page
  16. Artus J et al. (2011) The primitive endoderm lineage of the mouse blastocyst: sequential transcription factor activation and regulation of differentiation by Sox17. Dev Biol 350: 393-404 PubMed GONUTS page
  17. Chambers I et al. (2003) Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells. Cell 113: 643-55 PubMed GONUTS page
  18. Ivanova N et al. (2006) Dissecting self-renewal in stem cells with RNA interference. Nature 442: 533-8 PubMed GONUTS page
  19. 19.0 19.1 19.2 Kunarso G et al. (2008) Detailed characterization of the mouse embryonic stem cell transcriptome reveals novel genes and intergenic splicing associated with pluripotency. BMC Genomics 9: 155 PubMed GONUTS page
  20. Darr H et al. (2006) Overexpression of NANOG in human ES cells enables feeder-free growth while inducing primitive ectoderm features. Development 133: 1193-201 PubMed GONUTS page
  21. 21.0 21.1 Shimoda M et al. (2007) Sox17 plays a substantial role in late-stage differentiation of the extraembryonic endoderm in vitro. J Cell Sci 120: 3859-69 PubMed GONUTS page
  22. Pereira L et al. (2006) Repression of Nanog gene transcription by Tcf3 limits embryonic stem cell self-renewal. Mol Cell Biol 26: 7479-91 PubMed GONUTS page
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