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TMEM185A

Gene

transmembrane protein 185A

HGNCHGNC:17125EnsemblENSG00000269556NCBI Gene84548
Locus: gene with protein productLocation: Xq28

Also known as

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

Also known asCXorf13 · FAM11A · FRAXF
View full nomenclature history (6)
Previous symbolsCXorf13, FAM11A, FRAXF
Previous nameschromosome X open reading frame 13, family with sequence similarity 11, member A, fragile site, folic acid type, rare, fra(X)(q28) F

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.

Autistic Disorder
Child Development Disorders, Pervasive
Fragile X Syndrome
Ischemia

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 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.