FAM169A

Gene

family with sequence similarity 169 member A

HGNCHGNC:29138 EnsemblENSG00000198780 NCBI Gene26049

Locus: gene with protein productLocation: 5q13.3

Also known as

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

Also known asKIAA0888 · SLAP75 · SLAP

View full nomenclature history (6)

Alias symbolsKIAA0888, SLAP75, SLAP

Previous namesfamily with sequence similarity 169, member A

Alias namessoluble lamina-associated protein of 75 kD, Soluble-Lamin Associated Protein

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.

Anaphylaxis

Neuroendocrine Tumors

Depressive Disorder

Colorectal adenocarcinoma

Lung carcinoma

Carcinoma, Renal Cell

Systemic Inflammatory Response Syndrome

Intervertebral Disc Degeneration

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 2024-03-18.

Open TargetsGene–disease associations from the Open Targets Platform.