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WDR19


Official Full Name
WD repeat domain 19
Organism
Homo sapiens
Gene ID
57728
Background
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 glycine-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]
Synonyms
ATD5; CED4; DYF-2; FAP66; ORF26; Oseg6; PWDMP; SRTD5; CFAP66; IFT144; NPHP13; SPGF72

Cat.No. Product Name Price
SHH445960 shRNA set against Human WDR19 (NM_025132.3) Inquiry
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SHL130998 shRNA set against Mouse Wdr19(NM_153391.2) Inquiry
SHL131074 shRNA set against Human WDR19(NM_025132.3) Inquiry
Cat.No. Product Name Price
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CDCH100724 human WDR19 ORF clone (NM_025132.3) Inquiry
CDCH403884 Rat WDR19 ORF clone(NM_001191679.2) Inquiry
CDCR270294 Mouse Wdr19 ORF Clone(NM_153391.2) Inquiry
CDCS415906 Human WDR19 ORF Clone (BC032578) Inquiry
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