Wdr19 Gene Search Result

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2 records found for search term Wdr19

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1353133	WDR19	WD repeat domain 19	The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by g ... (more) lycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]	4	39182529	39285810	Human	519	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
628359280	WDR19-DT	WDR19 divergent transcript					Human		symbol , GTEx , COSMIC , name , Human Proteome Map	gene, ncrna