This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ARL13B-20-RE | 20 (40 μL) | 200 μL |  |
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| ARL13B-20-OR | 20 (40 μL) | 200 μL |  |
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| ARL13B-20-GO | 20 (40 μL) | 200 μL |  |
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| ARL13B-20-GR | 20 (40 μL) | 200 μL |  |
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| ARL13B-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
Gene Symbol : ARL13B
Gene Name : ADP ribosylation factor like GTPase 13B
Chromosome : CHR 3: 939,801,38-940,556,77
Locus : 3q11.1-q11.2
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