Synonyms:CIP98, DFNB31, ENTREZ:25861, HGNC:16361, MIM:607928, NM_001083885, NM_001173425, NM_001346890, NM_015404, NP_001077354, NP_001166896, NP_001333819, NP_056219, PDZD7B, USH2D, WHRN, WI, XM_011518485, XM_011518486, XM_011518487, XM_011518488, XM_011518489, XM_011518491, XM_011518492, XM_011518494, XP_011516787, XP_011516788, XP_011516789, XP_011516790, XP_011516791, XP_011516793, XP_011516794, XP_011516796, XR_929747, XR_929748, XR_929749, XR_929750, XR_929752, XR_929753, XR_929754, XR_929755, XR_929756, XR_929757, whirlin
Omim:OMIM:607928
Id:09c8eaa0-0189-5b54-8eb6-72aac5dae333
Hgnc:HGNC:16361
Description:whirlin
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]