CSHL1

Gene

chorionic somatomammotropin hormone like 1

HGNCHGNC:2442 EnsemblENSG00000204414 NCBI Gene1444

Locus: gene with protein productLocation: 17q23.3

Also known as

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

Also known asCSHP1 · hCS-L · CSL · CS-5 · MGC149868

View full nomenclature history (6)

Previous symbolsCSHP1

Alias symbolshCS-L, CSL, CS-5, MGC149868

Alias nameschorionic somatomammotropin CS-5

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.

46,XX gonadal dysgenesis

Primary Ovarian Insufficiency

Non-acquired isolated growth hormone deficiency

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.

Growth hormone 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.