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AXIN1 gene

axin 1

Key facts

Official symbol
AXIN1
Full name
AXIN1
Chromosome
16
Map location
16p13.3
Organism
Homo sapiens
NCBI Gene ID
8312
Also known as
AXIN, CMDOH, PPP1R49

Function summary

This gene encodes a cytoplasmic protein which contains a regulation of G-protein signaling (RGS) domain and a dishevelled and axin (DIX) domain. The encoded protein interacts with adenomatosis polyposis coli, catenin beta-1, glycogen synthase kinase 3 beta, protein phosphate 2, and itself. This protein functions as a negative regulator of the wingless-type MMTV integration site family, member 1 (WNT) signaling pathway and can induce apoptosis. The crystal structure of a portion of this protein, alone and in a complex with other proteins, has been resolved. Mutations in this gene have been associated with hepatocellular carcinoma, hepatoblastomas, ovarian endometriod adenocarcinomas, and medullablastomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016].

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Data source: NCBI Gene · alsesAI Gene Library