IGHMBP2

Gene

immunoglobulin mu DNA binding protein 2

HGNCHGNC:5542 EnsemblENSG00000132740 NCBI Gene3508

Locus: gene with protein productLocation: 11q13.3

Also known as

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

Also known asZFAND7 · SMUBP2 · CATF1 · SMARD1 · HCSA · HMN6 · CMT2S

View full nomenclature history (10)

Alias symbolsZFAND7, SMUBP2, CATF1, SMARD1, HCSA, HMN6, CMT2S

Previous namesimmunoglobulin mu binding protein 2

Alias namescardiac transcription factor 1, zinc finger, AN1-type domain 7

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.

Genetic Diseases, Inborn

Neurodegenerative Diseases

Charcot-Marie-Tooth Disease

Muscular Atrophy, Spinal

Neurodevelopmental Disorders

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.

Gene family

HGNC gene-group membership.

Zinc fingers AN1-typeUPF1 like RNA helicases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.