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MLIP

Gene

muscular LMNA interacting protein

HGNCHGNC:21355EnsemblENSG00000146147NCBI Gene90523
Locus: gene with protein productLocation: 6p12.1

Also known as

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

Also known asC6orf142 · MGC18257 · CIP
View full nomenclature history (6)
Previous symbolsC6orf142
Alias symbolsMGC18257, CIP
Previous nameschromosome 6 open reading frame 142
Alias namesmuscle-enriched A-type lamin interacting protein, cardiac ISL1-interacting protein

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.

Heart Failure
Heart Failure, Systolic
Cardiomyopathy, Hypertrophic
Placental abruption

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.

Provenance

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