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RIPOR2

Gene

RHO family interacting cell polarization regulator 2

HGNCHGNC:13872EnsemblENSG00000111913NCBI Gene9750
Locus: gene with protein productLocation: 6p22.3

Also known as

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

Also known asC6orf32 · FAM65B · KIAA0386 · DIFF48 · MYONAP
View full nomenclature history (8)
Previous symbolsC6orf32, FAM65B
Alias symbolsKIAA0386, DIFF48, MYONAP
Previous nameschromosome 6 open reading frame 32, family with sequence similarity 65 member B
Alias namesmyogenesis-related and NCAM-associated protein homolog (chicken)

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.

Hearing loss, autosomal recessive
Deafness
Nonsyndromic genetic hearing loss
Non-syndromic genetic deafness
Iron Metabolism Disorders
Arthritis, Rheumatoid
Dementia
Metabolic Diseases

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.

Armadillo like helical domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.