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Sequence Detail
ID/Version
D2J0Y4 (UniProt | EBI) Last sequence update: 2010-02-09
Last annotation update: 2024-05-29
Sequence
description
from provider
RecName: Full=(E2-independent) E3 ubiquitin-conjugating enzyme FATS {ECO:0000305}; EC=2.3.2.- {ECO:0000269|PubMed:24240685};AltName: Full=Centrosomal protein C10orf90 homolog {ECO:0000305};AltName: Full=E2/E3 hybrid ubiquitin-protein ligase FATS {
Provider SWISS-PROT
Sequence
Polypeptide 644 aa
For this sequence
Source
Organism mouse
See UniProt | EBI for 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.
Type Symbol Name GO Terms Expression
Assays
Orthologs Phenotypic
Alleles
Gene D7Ertd443e DNA segment, Chr 7, ERATO Doi 443, expressed 21 96 3 5
Sequence references in MGI J:160788 Li Z, et al., An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis. Oncogene. 2010 May 6;29(18):2659-71
J:175329 Zhang X, et al., FATS is a transcriptional target of p53 and associated with antitumor activity. Mol Cancer. 2010;9:244
J:265621 Yan S, et al., FATS is an E2-independent ubiquitin ligase that stabilizes p53 and promotes its activation in response to DNA damage. Oncogene. 2014 Nov 20;33(47):5424-33

Contributing Projects:
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
06/12/2024
MGI 6.13
The Jackson Laboratory