ID/Version |
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Sequence description from provider |
RecName: Full=Nuclear receptor-interacting protein 1;AltName: Full=Nuclear factor RIP140;AltName: Full=Receptor-interacting protein 140; | ||||||||||||||
Provider | SWISS-PROT | ||||||||||||||
Sequence |
Polypeptide
1161
aa
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Source | |||||||||||||||
Annotated genes and markers |
Follow the symbol links to get more information on the GO terms,
expression assays, orthologs, phenotypic alleles, and other information
for the genes or markers below.
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Sequence references in MGI |
J:50521
Lee CH, et al., Cloning and characterization of mouse RIP140, a corepressor for nuclear orphan receptor TR2. Mol Cell Biol. 1998 Nov;18(11):6745-55
J:74971 White R, et al., The nuclear receptor co-repressor nrip1 (RIP140) is essential for female fertility. Nat Med. 2000 Dec;6(12):1368-74 J:90688 Leonardsson G, et al., Nuclear receptor corepressor RIP140 regulates fat accumulation. Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8437-42 J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563 J:113776 Lee CH, et al., Characterization of receptor-interacting protein 140 in retinoid receptor activities. J Biol Chem. 1999 Oct 29;274(44):31320-6 J:113911 Wei LN, et al., Receptor-interacting protein 140 directly recruits histone deacetylases for gene silencing. J Biol Chem. 2000 Dec 29;275(52):40782-7 J:114064 Wei LN, et al., Ligand-dependent formation of retinoid receptors, receptor-interacting protein 140 (RIP140), and histone deacetylase complex is mediated by a novel receptor-interacting motif of RIP140. J Biol Chem. 2001 May 11;276(19):16107-12 J:114719 Huq MD, et al., Post-translational modification of nuclear co-repressor receptor-interacting protein 140 by acetylation. Mol Cell Proteomics. 2005 Jul;4(7):975-83 J:114726 Tullet JM, et al., Multiple signaling defects in the absence of RIP140 impair both cumulus expansion and follicle rupture. Endocrinology. 2005 Sep;146(9):4127-37 J:175152 Gupta P, et al., Retinoic acid-stimulated sequential phosphorylation, PML recruitment, and SUMOylation of nuclear receptor TR2 to suppress Oct4 expression. Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11424-9 J:213898 Poliandri AH, et al., Modulation of clock gene expression by the transcriptional coregulator receptor interacting protein 140 (RIP140). J Biol Rhythms. 2011 Jun;26(3):187-99 J:245382 Park SW, et al., SUMOylation of Tr2 orphan receptor involves Pml and fine-tunes Oct4 expression in stem cells. Nat Struct Mol Biol. 2007 Jan;14(1):68-75 J:254654 Vivante A, et al., A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling. J Am Soc Nephrol. 2017 Aug;28(8):2364-2376 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 03/18/2025 MGI 6.24 |
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