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ARL13B, ADP ribosylation factor like GTPase 13B

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ARL13B, ADP ribosylation factor like GTPase 13B

  • 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 Synonyms (ADP-ribosylation factor-like protein 13B, ADP-ribosylation factor-like 13B, ADP-ribosylation factor-like 2-like 1, ARL2-like protein 1, ARL2L1, JBTS8,)
  • NCBI Gene ID: 200894
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q3SXY8
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

ADP ribosylation factor like GTPase 13B interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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