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MCUR1

Gene

mitochondrial calcium uniporter regulator 1

HGNCHGNC:21097EnsemblENSG00000050393NCBI Gene63933
Locus: gene with protein productLocation: 6p23

Also known as

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

Also known asC6orf79 · CCDC90A · FLJ20958
View full nomenclature history (5)
Previous symbolsC6orf79, CCDC90A
Alias symbolsFLJ20958
Previous nameschromosome 6 open reading frame 79, coiled-coil domain containing 90A

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.

Muscular Atrophy
Wolff-Parkinson's-White syndrome
Pre-Eclampsia
Diabetic Ketoacidosis

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.

MCU complex subunits

Provenance

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