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MIMS1

Gene

mitochondrial inner membrane scaffold 1

HGNCHGNC:28346EnsemblENSG00000177150NCBI Gene125228
Locus: gene with protein productLocation: 18p11.21

Also known as

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

Also known asC18orf19 · FAM210A · MGC24180 · HsT2329
View full nomenclature history (6)
Previous symbolsC18orf19, FAM210A
Alias symbolsMGC24180, HsT2329
Previous nameschromosome 18 open reading frame 19, family with sequence similarity 210, member A

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.

Fractures, Bone
Ovarian dysfunction
Bone Diseases
Mucositis
Stomatitis
Osteoporosis
Hypothyroidism

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-06-12.
Open TargetsGene–disease associations from the Open Targets Platform.