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CEMIP

Gene

cell migration inducing hyaluronidase 1

HGNCHGNC:29213EnsemblENSG00000103888NCBI Gene57214
Locus: gene with protein productLocation: 15q25.1

Also known as

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

Also known asIR2155535 · TMEM2L · HYBID · CEMIP1
View full nomenclature history (8)
Alias symbolsIR2155535, TMEM2L, HYBID, CEMIP1
Previous namesKIAA1199, cell migration inducing protein, hyaluronan binding, cell migration inducing hyaluronan binding protein
Alias nameshyaluronan-binding protein involved in hyaluronan depolymerization

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.

Constriction, Pathologic
Pre-Eclampsia
Premature Birth
Idiopathic Pulmonary Fibrosis
Ovarian dysfunction
Iron Metabolism Disorders
Sleep Initiation and Maintenance Disorders
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.

Hyaluronidases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-02-05.
Open TargetsGene–disease associations from the Open Targets Platform.