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CYP1B1

Gene

cytochrome P450 family 1 subfamily B member 1

HGNCHGNC:2597EnsemblENSG00000138061NCBI Gene1545
Locus: gene with protein productLocation: 2p22.2

Also known as

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

Also known asGLC3A · CP1B
View full nomenclature history (4)
Previous symbolsGLC3A
Alias symbolsCP1B
Previous namescytochrome P450, subfamily I (dioxin-inducible), polypeptide 1 (glaucoma 3, primary infantile), cytochrome P450, family 1, subfamily B, polypeptide 1

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.

Congenital glaucoma
Basal cell carcinoma
Cutaneous melanoma
Skin Neoplasms

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.

Cytochrome P450 family 1Hydroperoxy icosatetraenoate dehydratases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-06-10.
Open TargetsGene–disease associations from the Open Targets Platform.