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CFC1B

Gene

cryptic, EGF-CFC family member 1B

HGNCHGNC:33983EnsemblENSG00000152093NCBI Gene653275
Locus: gene with protein productLocation: 2q21.1

Also known as

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

View full nomenclature history (1)
Previous namescripto, FRL-1, cryptic family 1B

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.

Heterotaxia
Visceral heterotaxy
Atrial septal defect

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.

EGF-CFC family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-06-05.
Open TargetsGene–disease associations from the Open Targets Platform.