Sequence Detail

ID/Version

Q9DCT2 Q8R073 Q8BTZ3 (UniProt | EBI)

Last sequence update: 2007-05-01
Last annotation update: 2024-03-27

Sequence description from provider

RecName: Full=NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial; EC=7.1.1.2 {ECO:0000269|PubMed:31916679, ECO:0000269|PubMed:33148885};AltName: Full=Complex I-30kD; Short=CI-30kD;AltName: Full=NADH-ubiquinone oxidoreduct

Provider

SWISS-PROT

Sequence

Polypeptide 263 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Ndufs3	NADH:ubiquinone oxidoreductase core subunit S3	35	98	3	12

Sequence references in MGI

J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:282679 Moutaoufik MT, et al., Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and Neurogenesis. iScience. 2019 Sep 27;19:1114-1132
J:285965 Pereira CV, et al., Myopathy reversion in mice after restauration of mitochondrial complex I. EMBO Mol Med. 2020 Feb 7;12(2):e10674
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:301995 Peralta S, et al., Metformin delays neurological symptom onset in a mouse model of neuronal complex I deficiency. JCI Insight. 2020 Nov 5;5(21)