BIVM

Gene

basic, immunoglobulin-like variable motif containing

HGNCHGNC:16034 EnsemblENSG00000134897 NCBI Gene54841

Locus: gene with protein productLocation: 13q33.1

Also known as

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

Also known asFLJ20159

View full nomenclature history (1)

Alias symbolsFLJ20159

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.

Autosomal dominant macrothrombocytopenia

MODY

Diabetes mellitus, transient neonatal, 3

Transient neonatal diabetes mellitus

Uncombable hair syndrome

Leukemia, Erythroblastic, Acute

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 2025-06-06.

Open TargetsGene–disease associations from the Open Targets Platform.