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ARL13B

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

ARL13B
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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.[5][6]

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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[7][8] and plays a role in cilia formation and in maintenance of cilia.[5]

Clinical significance

Mutations in the ARL13B gene are associated with the Joubert syndrome.[6]

References

Further reading

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