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TFCP2L1

Gene

transcription factor CP2 like 1

HGNCHGNC:17925EnsemblENSG00000115112NCBI Gene29842
Locus: gene with protein productLocation: 2q14.2

Also known as

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

Also known asLBP-9 · CRTR1
View full nomenclature history (3)
Alias symbolsLBP-9, CRTR1
Previous namestranscription factor CP2-like 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.

Neurodegenerative Diseases
Gout
Multiple Sclerosis
Alzheimer's Disease
Lysosomal Storage Diseases
Parkinson's Disease
Placental retention
Behcet's Syndrome
Depressive Disorder

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.

Transcription factor CP2 family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.