Synonyms:ENTREZ:23360, FBP30, FNBP4, HGNC:19752, MIM:615265, NM_001318339, NM_015308, NP_001305268, NP_056123, XM_024448408, XM_024448409, XP_024304176, XP_024304177, XR_001747804, XR_001747810, XR_001747813, XR_001747815, XR_002957134, XR_002957135, XR_002957136, XR_242785, XR_930854, XR_930855, formin binding protein 4
Omim:OMIM:615265
Id:ENSG00000109920
Hgnc:HGNC:19752
Description:formin binding protein 4
This gene encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome. [provided by RefSeq, Apr 2017]