intermembrane lipid transfer protein VPS13B isoform X10 [Rattus norveg - Protein

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Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport. [Am J Hum Genet. 2003]
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport.
Kolehmainen J, Black GC, Saarinen A, Chandler K, Clayton-Smith J, Träskelin AL, Perveen R, Kivitie-Kallio S, Norio R, Warburg M, et al. Am J Hum Genet. 2003 Jun; 72(6):1359-69. Epub 2003 May 2.
Gene and alternative splicing annotation with AIR. [Genome Res. 2005]
Gene and alternative splicing annotation with AIR.
Florea L, Di Francesco V, Miller J, Turner R, Yao A, Harris M, Walenz B, Mobarry C, Merkulov GV, Charlab R, et al. Genome Res. 2005 Jan; 15(1):54-66.

RefSeq mRNA
See reference mRNA sequence for the Vps13b gene (XM_039079222.2).
RefSeq protein isoforms
See 19 reference sequence protein isoforms for the Vps13b gene.

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Protein