Entrez gene ID | | 57539 |
Official gene symbol | | WDR35 |
Full name | | WD repeat domain 35 |
Aliases | | ,KIAA1336,MGC33196, |
Gene summary | | This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.[provided by RefSeq] |
Location | | Chromosome: 2 Locus: 2p24.1 |
Gene position | | 20189884 - 20110024 Map Viewer |
Gene orientation | | minus |
Gene size | | 79861 bp |
Gene sequence |
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OMIM ID | | 613602 |
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