| NDUFS4 | 
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| Identifiers | 
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| Aliases | NDUFS4, AQDQ, CI-18, CI-18 kDa, CI-AQDQ, NADH:ubiquinone oxidoreductase subunit S4, MC1DN1 | 
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| External IDs | OMIM: 602694; MGI: 1343135; HomoloGene: 1866; GeneCards: NDUFS4; OMA:NDUFS4 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 13 (mouse) | 
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 |  |  | Band | 13|13 D2.2 | Start | 114,424,331 bp | 
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 | End | 114,524,794 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | Achilles tendon
 Skeletal muscle tissue of rectus abdominis
 muscle of thigh
 gastrocnemius muscle
 thoracic diaphragm
 body of tongue
 biceps brachii
 left ventricle
 apex of heart
 Skeletal muscle tissue of biceps brachii
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 | | Top expressed in |  | intercostal muscle
 digastric muscle
 temporal muscle
 right ventricle
 muscle of thigh
 sternocleidomastoid muscle
 right kidney
 triceps brachii muscle
 ventricular zone
 medial ganglionic eminence
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial (NDUFS4) also known as NADH-ubiquinone oxidoreductase 18 kDa subunit is an enzyme that in humans is encoded by the NDUFS4 gene. This gene encodes a nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome.