ZNF722

Gene

zinc finger protein 722

HGNCHGNC:22571 EnsemblENSG00000241149 NCBI Gene100419780

Locus: gene with protein productLocation: 7q11.21

Also known as

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

Also known asZNF722P

View full nomenclature history (2)

Previous symbolsZNF722P

Previous nameszinc finger protein 722, pseudogene

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.

immunoglobulin G4-related sclerosing disease

Leber Congenital Amaurosis

Early-onset non-syndromic cataract

Congenital glaucoma

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 C2H2-typeKRAB domain containing

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.