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NUBPL

Gene

NUBP iron-sulfur cluster assembly factor, mitochondrial

HGNCHGNC:20278EnsemblENSG00000151413NCBI Gene80224
Locus: gene with protein productLocation: 14q12

Also known as

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

Also known asC14orf127 · FLJ12660 · IND1 · huInd1
View full nomenclature history (8)
Previous symbolsC14orf127
Alias symbolsFLJ12660, IND1, huInd1
Previous nameschromosome 14 open reading frame 127, nucleotide binding protein-like, nucleotide binding protein like
Alias namesiron-sulfur protein required for NADH dehydrogenase

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.

Mitochondrial Diseases
Neurodegenerative Diseases
Genetic Diseases, Inborn
Myasthenia Gravis
Alcohol drinking
Pericarditis

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.

Mitochondrial respiratory chain complex assembly factorsMitochondrial iron-sulfur assembly components

Provenance

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