ARL13B
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). ADP-ribosylation factor-like protein 13B (ARL13B), also known as ADP-ribosylation factor-like protein 2-like 1, is a protein that in humans is encoded by the ARL13B gene.[1][2]
Function
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[3] [4] and plays a role in cilia formation and in maintenance of cilia.[1]
Clinical significance
Mutations in the ARL13B gene are associated with the Joubert syndrome.[2]
References
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<references />, or <references group="..." />Further reading
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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