| 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.