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ADAM9

Gene

ADAM metallopeptidase domain 9

HGNCHGNC:216EnsemblENSG00000168615NCBI Gene8754
Locus: gene with protein productLocation: 8p11.22

Also known as

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

Also known asCORD9 · MDC9 · KIAA0021 · MCMP · Mltng
View full nomenclature history (8)
Previous symbolsCORD9
Alias symbolsMDC9, KIAA0021, MCMP, Mltng
Previous namesa disintegrin and metalloproteinase domain 9 (meltrin gamma), cone rod dystrophy 9
Alias namesmeltrin gamma

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.

Cone rod dystrophy
Cone-rod dystrophy
Eye Diseases
Retinitis Pigmentosa

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.

ADAM metallopeptidase domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.