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Proteintech
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Immunogen sequence: MFSLMASCCG WFKRWREPVR LANKQDKEGA LGEADVIECL SLEKLVNEHK CLCQIEPCSA ISGYGKKIDK SIKKGLYWLL HVIARDFDAL NERIQKETTE QRALEEQEKQ ERAERVRKLR EERKQNEQEQ AELDGTSGLA ELDPEPTNPF QPIASVIIEN EGKLEREKKN QKMEKDSDGC HLKHKMEHEQ IETQGQVNHN GQKNNEFGLV ENYKEALTQQ LKNEDETDRP SLESANGKKK TKKLRMKRNH RVEPLNIDDC APESPTPPPP PPPVGWGTPK VTRLPKLEPL GETHHNDFYR KPLPPLAVPQ RPNSDAHDVI S
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 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
基因别名: ARL13B; ARL2L1; JBTS8
UniProt ID: (Human) Q3SXY8
Entrez Gene ID: (Human) 200894