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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for WDR35 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID57539
Official gene symbolWDR35
Full nameWD repeat domain 35
Aliases,KIAA1336,MGC33196,
Gene summaryThis 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]
LocationChromosome: 2   Locus: 2p24.1
Gene position20189884 - 20110024  Map Viewer
Gene orientationminus
Gene size79861 bp
Gene sequence
OMIM ID613602