RAB5B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | RAB5B , Rab-5B, member RAS oncogene family | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 179514 MGI: 105938 HomoloGene: 104027 GeneCards: RAB5B | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Ras-related protein Rab-5B is a protein that in humans is encoded by the RAB5B gene. [5] [6] [7]
Ras-related protein Rab-4A is a protein that in humans is encoded by the RAB4A gene.
Spermatid perinuclear RNA-binding protein is a protein that in humans is encoded by the STRBP gene.
Ras guanyl-releasing protein 3 is a protein that in humans is encoded by the RASGRP3 gene.
ADP-ribosylation factor-like protein 1 is a protein that in humans is encoded by the ARL1 gene.
Ras-related protein Rab-17 is a protein that in humans is encoded by the RAB17 gene.
Myotubularin-related protein 6 is a protein that in humans is encoded by the MTMR6 gene.
USP6 N-terminal-like protein is a protein that in humans is encoded by the USP6NL gene.
Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.
Uncharacterized protein KIAA1267 is a protein that in humans is encoded by the KIAA1267 gene.
Rho guanine nucleotide exchange factor (GEF) 3, also known as ARHGEF3, is a human gene.
LisH domain-containing protein ARMC9 is a protein that in humans is encoded by the ARMC9 gene.
Hippocalcin like 4, also known as HPCAL4, is a human gene.
Large subunit GTPase 1 homolog is an enzyme that in humans is encoded by the LSG1 gene.
AP-1 complex-associated regulatory protein is a protein that in humans is encoded by the AP1AR gene.
Probable ATP-dependent RNA helicase DDX43 is an enzyme that in humans is encoded by the DDX43 gene.
Synaptotagmin-13 is a protein that in humans is encoded by the SYT13 gene.
Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair. Ruijs-Aalfs syndrome is an autosomal recessive genetic disorder. Characteristics of this disorder are features of premature aging, chromosome instability and development of hepatocellular carcinoma. Ruijs-Aalfs syndrome arises as a result of mutations in the SPRTN gene that encodes a metalloproteinase employed in the repair of protein-linked DNA breaks.
Zinc finger protein 34 is a protein that in humans is encoded by the ZNF34 gene.
Ankyrin repeat domain-containing protein 13C is a protein that in humans is encoded by the ANKRD13C gene.
Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene. Leiomodin-3 is especially present at the pointed end of muscle thin filaments.