RAB7A

Gene

RAB7A, member RAS oncogene family

HGNCHGNC:9788 EnsemblENSG00000075785 NCBI Gene7879

Locus: gene with protein productLocation: 3q21.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asRAB7 · CMT2B

View full nomenclature history (4)

Previous symbolsRAB7, CMT2B

Previous namesRAB7, member RAS oncogene family, Charcot-Marie-Tooth neuropathy 2B

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Neurodegenerative Diseases

Parkinson's Disease

Tuberculosis

Alzheimer's Disease

Lysosomal Storage Diseases

Multiple Sclerosis

Autoimmune disorder of central nervous system

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

RAB, member RAS oncogene GTPases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.