NDUFB9

From Wikipedia, the free encyclopedia

NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa

Identifiers

NDUFB9; B22; DKFZp566O173; FLJ22885; LYRM3; UQOR22

External IDs

OMIM: 601445 MGI: 1913468 HomoloGene: 3669

Gene ontology
Molecular Function:	• NADH dehydrogenase activity • NADH dehydrogenase (ubiquinone) activity • oxidoreductase activity
Cellular Component:	• mitochondrion • mitochondrial inner membrane
Biological Process:	• mitochondrial electron transport, NADH to ubiquinone • sensory perception of sound

Orthologs

Human

Mouse

Refseq

NM_005005 (mRNA)
NP_004996 (protein)

NM_023172 (mRNA)
NP_075661 (protein)

Location

Chr 8: 125.62 - 125.63 Mb

Chr 15: 58.76 - 58.77 Mb

Pubmed search

[1]

[2]

NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa, also known as NDUFB9, is a human gene.^[1]

[edit] References

^ Entrez Gene: NDUFB9 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa.

[edit] Further reading

Gu JZ, Lin X, Wells DE (1996). "The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome.". Genomics 35 (1): 6-10. doi:10.1006/geno.1996.0316. PMID 8661098.
Emahazion T, Beskow A, Gyllensten U, Brookes AJ (1998). "Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain.". Cytogenet. Cell Genet. 82 (1-2): 115-9. PMID 9763677.
Loeffen JL, Triepels RH, van den Heuvel LP, et al. (1999). "cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.". Biochem. Biophys. Res. Commun. 253 (2): 415-22. doi:10.1006/bbrc.1998.9786. PMID 9878551.
Lin X, Wells DE, Kimberling WJ, Kumar S (1999). "Human NDUFB9 gene: genomic organization and a possible candidate gene associated with deafness disorder mapped to chromosome 8q13.". Hum. Hered. 49 (2): 75-80. PMID 10077726.
Dias Neto E, Correa RG, Verjovski-Almeida S, et al. (2000). "Shotgun sequencing of the human transcriptome with ORF expressed sequence tags.". Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3491-6. PMID 10737800.
Ye Z, Connor JR (2000). "cDNA cloning by amplification of circularized first strand cDNAs reveals non-IRE-regulated iron-responsive mRNAs.". Biochem. Biophys. Res. Commun. 275 (1): 223-7. doi:10.1006/bbrc.2000.3282. PMID 10944468.
Zhang QH, Ye M, Wu XY, et al. (2001). "Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells.". Genome Res. 10 (10): 1546-60. PMID 11042152.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome.". Cell 122 (6): 957-68. doi:10.1016/j.cell.2005.08.029. PMID 16169070.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173-8. doi:10.1038/nature04209. PMID 16189514.