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MARVELD2

Gene

MARVEL domain containing 2

HGNCHGNC:26401EnsemblENSG00000152939NCBI Gene153562
Locus: gene with protein productLocation: 5q13.2

Also known as

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

Also known asMRVLDC2 · DFNB49 · FLJ30532 · TRIC
View full nomenclature history (7)
Previous symbolsMRVLDC2, DFNB49
Alias symbolsFLJ30532, TRIC
Previous namesMARVEL (membrane-associating) domain containing 2, deafness, autosomal recessive 49
Alias namestricellulin

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
Non-syndromic genetic deafness
Hearing Loss
Nonsyndromic genetic hearing loss
Neurodegenerative 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.

MARVEL 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.