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MAGEE2

Gene

MAGE family member E2

HGNCHGNC:24935EnsemblENSG00000186675NCBI Gene139599
Locus: gene with protein productLocation: Xq13.3

Also known as

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

Also known asHCA3
View full nomenclature history (4)
Alias symbolsHCA3
Previous namesmelanoma antigen family E2
Alias namesMelanoma-associated antigen E2, Hepatocellular carcinoma-associated protein 3

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.

Genetic central nervous system malformation
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Polymicrogyria due to TUBB2B mutation
Genetic developmental and epileptic encephalopathy

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.

MAGE family

Provenance

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