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Protein-coding gene in the species Homo sapiens
by the NDUFAF6 gene. The protein is involved in the assembly of complex I in the mitochondrial electron transport chain. Mutations in the NDUFAF6 gene have
NDUFAF6
Metabolic disease
NDUFA10); chromosome 5 (SDHA, NDUFS4, NDUFAF2, and NDUFA2); chromosome 8 (NDUFAF6), chromosome 10 (COX15); chromosome 11 (NDUFS3, NDUFS8, and FOXRED1); chromosome
Leigh_syndrome
Muscle disorders caused by mitochondrial dysfunction
NDUFAF3, TIMMDC1, ACAD9, NDUFS6, NDUFS4, NDUFAF2, NDUFA2, NDUFAF4, DNAJC30, NDUFAF6, NDUFB9, NDUFA8, NDUFB8, NDUFS3, NDUFV1, NDUFS8, NDUFC2, TMEM126B, FOXRED1
Mitochondrial_myopathy
10368 NDUFAF4 HGNC:21034; Q9P032 10369 NDUFAF5 HGNC:15899; Q5TEU4 10370 NDUFAF6 HGNC:28625; Q330K2 10371 NDUFAF7 HGNC:28816; Q7L592 10372 NDUFAF8 HGNC:33551;
List of human protein-coding genes 5
List_of_human_protein-coding_genes_5
Gene on human chromosome 10
susceptibility 2 (ARMS2), and NADH dehydrogenase complex I assembly factor 6 (NDUFAF6). BTBD16 has been found in species as far back as cartilaginous fishes
BTBD16
NDUFAF6
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