Species Human Entrez 9750 | Human Mouse Ensembl ENSG00000111913 | |
Aliases FAM65B, C6orf32, DIFF40, DIFF48, MYONAP, PL48, DFNB104, family with sequence similarity 65 member B External IDs MGI: 2444879 HomoloGene: 9284 GeneCards: FAM65B | ||
Family with sequence similarity 65, member B is a protein that in humans is encoded by the FAM65B gene.
Contents
Function
The protein encoded by this gene stimulates the formation of a non-mitotic multinucleate syncytium from proliferative cytotrophoblasts during trophoblast differentiation. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2013].
Clinical significance
Mutations in FAM65B are associated to hearing loss .
References
FAM65B Wikipedia(Text) CC BY-SA