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Immunogen sequence: MFSLMASCC GWFKRWREPV RLANKQDKEG ALGEADVIEC LSLEKLVNEH KCLCQIEPCS AISGYGKKID KSIKKGLYWL LHVIARDFDA LNERIQKETT EQRALEEQEK QERAERVRKL REERKQNEQE QAELDGTSGL AELDPEPTNP FQPIASVIIE NEGKLEREKK NQKMEKDSDG CHLKHKMEHE QIETQGQVNH NGQKNNEFGL VENYKEALTQ QLKNEDETDR PSLESANGKK KTKKLRMKRN HRVEPLNIDD CAPESPTPPP PPPPVGWGTP KVTRLPKLEP LGETHHNDFY RKPLPPLAVP QRPNSDAHDV IS (1-321 aa encoded by BC094725)
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ADP-ribosylation factor like GTPase 13B; ADP-ribosylation factor-like 13B; ADP-ribosylation factor-like 2-like 1; ADP-ribosylation factor-like protein 13B; ADP-ribosylation factor-like protein 2-like 1; ARL2-like protein 1; Protein hennin
Gene Aliases: A530097K21Rik; A930014M17Rik; ARL13B; ARL2L1; C530009C10Rik; hnn; JBTS8
UniProt ID: (Human) Q3SXY8, (Mouse) Q640N2
Entrez Gene ID: (Dog) 487934, (Pig) 100624385, (Human) 200894, (Mouse) 68146
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