POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutations in this gene result in short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT) syndrome. [provided by RefSeq, Sep 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| POC1A-20-RE | 20 (40 μL) | 200 μL |  |
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| POC1A-20-OR | 20 (40 μL) | 200 μL |  |
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| POC1A-20-GO | 20 (40 μL) | 200 μL |  |
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| POC1A-20-GR | 20 (40 μL) | 200 μL |  |
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| POC1A-20-AQ | 20 (40 μL) | 200 μL |  |
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POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutations in this gene result in short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT) syndrome. [provided by RefSeq, Sep 2012]
Gene Symbol : POC1A
Gene Name : POC1 centriolar protein A
Chromosome : CHR 3: 521,546,89-520,752,32
Locus : 3p21.2
Alt. Genes : OPTN
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