RAB7A

RAB7A
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRAB7A, PRO2706, RAB7, member RAS oncogene family, CMT2B
External IDsOMIM: 602298; MGI: 105068; HomoloGene: 3408; GeneCards: RAB7A; OMA:RAB7A - orthologs
Orthologs
SpeciesHumanMouse
Entrez

7879

19349

Ensembl

ENSG00000075785

ENSMUSG00000079477

UniProt

P51149

P51150

RefSeq (mRNA)

NM_004637

NM_001293652
NM_001293653
NM_001293654
NM_001293655
NM_009005

RefSeq (protein)

NP_004628

NP_001280581
NP_001280582
NP_001280583
NP_001280584
NP_033031

Location (UCSC)Chr 3: 128.69 – 128.83 MbChr 6: 87.98 – 88.02 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Ras-related protein Rab-7a is a protein that in humans is encoded by the RAB7A gene.

Ras-related protein Rab-7a is involved in endocytosis, which is a process that brings substances into a cell. The process of endocytosis works by folding the cell membrane around a substance outside of the cell (for example a protein) and then forms a vesicle. The vesicle is then brought into the cell and cleaved from the cell membrane. RAB7A plays an important role in the movement of vesicles into the cell as well as with vesicle trafficking.

Various mutations of RAB7A are associated with Hereditary sensory neuropathy type 1C (HSN IC), also known as Charcot-Marie-Tooth syndrome type 2B (CMT2B).