pcdh15 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description protocadherin-related 15|This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008] (NCBI Entrez Gene Database, 65217)
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Genes

6 genes co-occuring with the biological term pcdh15 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
CDH23 cadherin-related 23
MYH14 myosin, heavy chain 14, non-muscle
MYO7A myosin VIIA
PCDH15 protocadherin-related 15
USH2A Usher syndrome 2A (autosomal recessive, mild)