NDUFAF6

NDUFAF6
Identifiers
Aliases	NDUFAF6, C8orf38, NADH:ubiquinone oxidoreductase complex assembly factor 6
External IDs	OMIM: 612392 MGI: 1924197 HomoloGene: 43831 GeneCards: NDUFAF6
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	11,076,205 bp
Gene ontology
Molecular function	• transferase activity;
Cellular component	• nucleus; • membrane; • cytoplasm; • mitochondrion; • mitochondrial inner membrane;
Biological process	• mitochondrial respiratory chain complex I assembly; • biosynthetic process;
	Sources:Amigo / QuickGO
Orthologs
	137682
	76947
	ENSG00000156170
	ENSMUSG00000050323
	Q330K2
	A2AIL4
	NM_152416; NM_001330582
	NM_001085493
NP_001317511; NP_689629; NP_001341443; NP_001341444; NP_001341445;
	NP_001341446; NP_001341447; NP_001341448; NP_001341450; NP_001341451; NP_001341453; NP_001341456; NP_001341457; NP_001341458; NP_001341460; NP_001341461; NP_001341462; NP_001341463; NP_001341454; NP_001341459
	NP_001078962
	Wikidata
View/Edit Human	View/Edit Mouse

NADH:ubiquinone oxidoreductase complex assembly factor 6 is a protein that in humans is encoded by the NDUFAF6 gene. The protein is involved in the assembly of complex I in the mitochondrial electron transport chain.^[4] Mutations in the NDUFAF6 gene have been shown to cause Complex I deficiency, Leigh syndrome, and Acadian variant Fanconi Syndrome.^[5]

Structure[]

The NDUFAF6 gene is located on the q arm of chromosome 8 in position 22.1 and spans 222,728 base pairs.^[4] The gene produces a 38.2 kDa protein composed of 333 amino acids.^[6]^[7] The protein contains a predicted phytoene synthase domain.^[4]

Function[]

The NDUFAF6 gene encodes a protein that localizes to mitochondria. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis.^[4]

Clinical Significance[]

Mutations in the NDUFAF6 gene are associated with complex I enzymatic deficiency^[4] and lead to Leigh syndrome,^[8] which is characterized by lesions in the central nervous system and rapid deterioration of cognitive and motor functions. In Acadians, a non-coding mutation in NDUFAF6 has been shown to cause Acadian variant Fanconi Syndrome, symptoms of which include pulmonary interstitial fibrosis and proximal tubular dysfunction accompanied by slowly progressive kidney disease. Inheritance of mutations in the NDUFAF6 gene is autosomal recessive.^[5]

Interactions[]

The protein encoded by NDUFAF6 interacts with RHOXF2, OTX1, GUCD1,^[9] and GALNT6^[10] proteins.

References[]

^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000050323 - Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ ^a ^b ^c ^d ^e "Entrez Gene: NADH:ubiquinone oxidoreductase complex assembly factor 6". Retrieved 2018-07-25.
^ ^a ^b Bianciardi, Laura; Imperatore, Valentina; Fernandez-Vizarra, Erika; Lopomo, Angela; Falabella, Micol; Furini, Simone; Galluzzi, Paolo; Grosso, Salvatore; Zeviani, Massimo (2016). "Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene". Molecular Genetics and Metabolism. 119 (3): 214–222. doi:10.1016/j.ymgme.2016.09.001. ISSN 1096-7192. PMID 27623250.
^ Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (Oct 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
^ "NDUFAF6 - NADH dehydrogenase (ubiquinone) complex I, assembly factor 6". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB).
^ Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: {612392}: {04/29/2015}: . World Wide Web URL: https://omim.org/
^ IntAct. "id:Q330K2*". www.ebi.ac.uk. Retrieved 2018-07-26.
^ Lab, Mike Tyers. "NDUFAF6 Result Summary | BioGRID". thebiogrid.org. Retrieved 2018-07-26.

Further reading[]

Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ (September 2010). "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression". PLOS ONE. 5 (9): e12862. Bibcode:2010PLoSO...512862H. doi:10.1371/journal.pone.0012862. PMC 2943476. PMID 20877624.
McKenzie M, Tucker EJ, Compton AG, Lazarou M, George C, Thorburn DR, Ryan MT (December 2011). "Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1". J. Mol. Biol. 414 (3): 413–26. doi:10.1016/j.jmb.2011.10.012. PMID 22019594.
Zhang K, Li Z, Jaiswal M, Bayat V, Xiong B, Sandoval H, Charng WL, David G, Haueter C, Yamamoto S, Graham BH, Bellen HJ (March 2013). "The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit". J. Cell Biol. 200 (6): 807–20. doi:10.1083/jcb.201208033. PMC 3601355. PMID 23509070.
Hartmannová H, Piherová L, Tauchmannová K, Kidd K, Acott PD, Crocker JF, Oussedik Y, Mallet M, Hodaňová K, Stránecký V, Přistoupilová A, Barešová V, Jedličková I, Živná M, Sovová J, Hůlková H, Robins V, Vrbacký M, Pecina P, Kaplanová V, Houštěk J, Mráček T, Thibeault Y, Bleyer AJ, Kmoch S (September 2016). "Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6". Hum. Mol. Genet. 25 (18): 4062–4079. doi:10.1093/hmg/ddw245. PMID 27466185.
Bianciardi L, Imperatore V, Fernandez-Vizarra E, Lopomo A, Falabella M, Furini S, Galluzzi P, Grosso S, Zeviani M, Renieri A, Mari F, Frullanti E (November 2016). "Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene". Mol. Genet. Metab. 119 (3): 214–222. doi:10.1016/j.ymgme.2016.09.001. PMID 27623250.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

[refGRCm38Ensembl-1] GRCm38: Ensembl release 89: ENSMUSG00000050323 - Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[3] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-4] "Entrez Gene: NADH:ubiquinone oxidoreductase complex assembly factor 6". Retrieved 2018-07-25.

[:1-5] Bianciardi, Laura; Imperatore, Valentina; Fernandez-Vizarra, Erika; Lopomo, Angela; Falabella, Micol; Furini, Simone; Galluzzi, Paolo; Grosso, Salvatore; Zeviani, Massimo (2016). "Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene". Molecular Genetics and Metabolism. 119 (3): 214–222. doi:10.1016/j.ymgme.2016.09.001. ISSN 1096-7192. PMID 27623250.

[COPaKB-6] Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (Oct 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.

[url_COPaKB-7] "NDUFAF6 - NADH dehydrogenase (ubiquinone) complex I, assembly factor 6". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB).

[:0-8] Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: {612392}: {04/29/2015}: . World Wide Web URL: https://omim.org/

[9] IntAct. "id:Q330K2*". www.ebi.ac.uk. Retrieved 2018-07-26.

[10] Lab, Mike Tyers. "NDUFAF6 Result Summary | BioGRID". thebiogrid.org. Retrieved 2018-07-26.

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