ID/Version |
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Sequence description from provider |
RecName: Full=Tumor protein 63; Short=p63;AltName: Full=Transformation-related protein 63; Short=TP63;AltName: Full=Tumor protein p73-like; Short=p73L; | ||||||||||||||
Provider | SWISS-PROT | ||||||||||||||
Sequence |
Polypeptide
680
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:45977
Senoo M, et al., A second p53-related protein, p73L, with high homology to p73 [published erratum appears in Biochem Biophys Res Commun 1998 Sep 18;250(2):536]. Biochem Biophys Res Commun. 1998 Jul 30;248(3):603-7
J:50106 Yang A, et al., p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell. 1998 Sep;2(3):305-16 J:54636 Mills AA, et al., p63 is a p53 homologue required for limb and epidermal morphogenesis. Nature. 1999 Apr 22;398(6729):708-13 J:54637 Yang A, et al., p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature. 1999 Apr 22;398(6729):714-8 J:77565 Flores ER, et al., p63 and p73 are required for p53-dependent apoptosis in response to DNA damage. Nature. 2002 Apr 4;416(6880):560-4 J:87781 Koster MI, et al., p63 is the molecular switch for initiation of an epithelial stratification program. Genes Dev. 2004 Jan 15;18(2):126-31 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:183160 Mitchell K, et al., Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus. Am J Hum Genet. 2012 Jan 13;90(1):69-75 J:297664 Simonson L, et al., Keratin 13 deficiency causes white sponge nevus in mice. Dev Biol. 2020 Dec 1;468(1-2):146-153 J:333827 Huang C, et al., TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosis. J Clin Invest. 2023 Mar 1;133(5) |
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 11/12/2024 MGI 6.24 |
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