FAM171A1

Gene

family with sequence similarity 171 member A1

HGNCHGNC:23522 EnsemblENSG00000148468 NCBI Gene221061

Locus: gene with protein productLocation: 10p13

Also known as

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

Also known asC10orf38 · FLJ12884 · APCN

View full nomenclature history (6)

Previous symbolsC10orf38

Alias symbolsFLJ12884, APCN

Previous nameschromosome 10 open reading frame 38, family with sequence similarity 171, member A1

Alias namesastroprincin

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.

Alcohol drinking

Amino Acid Metabolism, Inborn Errors

Rotator cuff syndrome

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 2026-07-06.

Open TargetsGene–disease associations from the Open Targets Platform.