Gene: WDR35

Alternate names for this Gene: CED2|FAP118|IFT121|IFTA1|SRTD7

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.

Gene is located in Chromosome: 2

Location in Chromosome : 2p24.1

Description of this Gene: WD repeat domain 35

Type of Gene: protein-coding

Gene: LOC101928222

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 2

Location in Chromosome : 2p24.1

Description of this Gene: uncharacterized LOC101928222

Type of Gene: ncRNA