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NSL1

Gene

NSL1 component of MIS12 kinetochore complex

HGNCHGNC:24548EnsemblENSG00000117697NCBI Gene25936
Locus: gene with protein productLocation: 1q32.3

Also known as

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

Also known asC1orf48 · DC8 · DKFZP566O1646 · MIS14
View full nomenclature history (7)
Previous symbolsC1orf48
Alias symbolsDC8, DKFZP566O1646, MIS14
Previous namesNSL1, MIND kinetochore complex component, homolog (S. cerevisiae), chromosome 1 open reading frame 48, NSL1, MIS12 kinetochore complex component

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
Thyroid Diseases
Malaria
Hypothyroidism
Childhood onset asthma
Brain Neoplasms
Cutaneous mastocytosis
Neoplasms
Anemia

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.

MIS12 kinetochore complex

Provenance

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