2025-05-09 18:50:26, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_004376 6450 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens cytochrome c oxidase assembly homolog 15 (yeast) (COX15), transcript variant 2, mRNA. ACCESSION NM_004376 VERSION NM_004376.5 GI:189011539 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 6450) AUTHORS Comuzzie,A.G., Cole,S.A., Laston,S.L., Voruganti,V.S., Haack,K., Gibbs,R.A. and Butte,N.F. TITLE Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population JOURNAL PLoS ONE 7 (12), E51954 (2012) PUBMED 23251661 REFERENCE 2 (bases 1 to 6450) AUTHORS Kenny,E.E., Pe'er,I., Karban,A., Ozelius,L., Mitchell,A.A., Ng,S.M., Erazo,M., Ostrer,H., Abraham,C., Abreu,M.T., Atzmon,G., Barzilai,N., Brant,S.R., Bressman,S., Burns,E.R., Chowers,Y., Clark,L.N., Darvasi,A., Doheny,D., Duerr,R.H., Eliakim,R., Giladi,N., Gregersen,P.K., Hakonarson,H., Jones,M.R., Marder,K., McGovern,D.P., Mulle,J., Orr-Urtreger,A., Proctor,D.D., Pulver,A., Rotter,J.I., Silverberg,M.S., Ullman,T., Warren,S.T., Waterman,M., Zhang,W., Bergman,A., Mayer,L., Katz,S., Desnick,R.J., Cho,J.H. and Peter,I. TITLE A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci JOURNAL PLoS Genet. 8 (3), E1002559 (2012) PUBMED 22412388 REFERENCE 3 (bases 1 to 6450) AUTHORS Hendrickson,S.L., Lautenberger,J.A., Chinn,L.W., Malasky,M., Sezgin,E., Kingsley,L.A., Goedert,J.J., Kirk,G.D., Gomperts,E.D., Buchbinder,S.P., Troyer,J.L. and O'Brien,S.J. TITLE Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression JOURNAL PLoS ONE 5 (9), E12862 (2010) PUBMED 20877624 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) Publication Status: Online-Only REFERENCE 4 (bases 1 to 6450) AUTHORS Vitali,M., Venturelli,E., Galimberti,D., Benerini Gatta,L., Scarpini,E. and Finazzi,D. TITLE Analysis of the genes coding for subunit 10 and 15 of cytochrome c oxidase in Alzheimer's disease JOURNAL J Neural Transm 116 (12), 1635-1641 (2009) PUBMED 19826901 REMARK GeneRIF: COX 15 mRNA was significantly more abundant in the cerebral tissue of Alzheimer's disease (AD) patients and COX10 and COX15 SNP were significantly less represented in the patient group, suggesting a possible protective role toward the risk for AD GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 5 (bases 1 to 6450) AUTHORS Dassa,E.P., Dufour,E., Goncalves,S., Paupe,V., Hakkaart,G.A., Jacobs,H.T. and Rustin,P. TITLE Expression of the alternative oxidase complements cytochrome c oxidase deficiency in human cells JOURNAL EMBO Mol Med 1 (1), 30-36 (2009) PUBMED 20049701 REMARK GeneRIF: The expression of the AOX, well-tolerated by the cells, compensates for both the growth defect and the pronounced oxidant-sensitivity of COX-deficient human cells. REFERENCE 6 (bases 1 to 6450) AUTHORS Oquendo,C.E., Antonicka,H., Shoubridge,E.A., Reardon,W. and Brown,G.K. TITLE Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome JOURNAL J. Med. Genet. 41 (7), 540-544 (2004) PUBMED 15235026 REMARK GeneRIF: A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene. REFERENCE 7 (bases 1 to 6450) AUTHORS Antonicka,H., Mattman,A., Carlson,C.G., Glerum,D.M., Hoffbuhr,K.C., Leary,S.C., Kennaway,N.G. and Shoubridge,E.A. TITLE Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy JOURNAL Am. J. Hum. Genet. 72 (1), 101-114 (2003) PUBMED 12474143 REMARK GeneRIF: Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy REFERENCE 8 (bases 1 to 6450) AUTHORS Barros,M.H., Carlson,C.G., Glerum,D.M. and Tzagoloff,A. TITLE Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O JOURNAL FEBS Lett. 492 (1-2), 133-138 (2001) PUBMED 11248251 REFERENCE 9 (bases 1 to 6450) AUTHORS Petruzzella,V., Tiranti,V., Fernandez,P., Ianna,P., Carrozzo,R. and Zeviani,M. TITLE Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain JOURNAL Genomics 54 (3), 494-504 (1998) PUBMED 9878253 REFERENCE 10 (bases 1 to 6450) AUTHORS Kennaway,N.G., Carrero-Valenzuela,R.D., Ewart,G., Balan,V.K., Lightowlers,R., Zhang,Y.Z., Powell,B.R., Capaldi,R.A. and Buist,N.R. TITLE Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency JOURNAL Pediatr. Res. 28 (5), 529-535 (1990) PUBMED 2175025 REMARK Review article COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BX537557.1, DB094258.1, AF044323.1, BC078161.1 and AL133353.6. This sequence is a reference standard in the RefSeqGene project. On May 22, 2008 this sequence version replaced gi:156071495. Summary: Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be essential for the biogenesis of COX formation and may function in the hydroxylation of heme O, according to the yeast mutant studies. This protein is predicted to contain 5 transmembrane domains localized in the mitochondrial inner membrane. Alternative splicing of this gene generates two transcript variants diverging in the 3' region. [provided by RefSeq, Jul 2008]. Transcript Variant: This variant (2) lacks an internal segment in the 3' region, as compared to variant 1. The encoded isoform 2 has a shorter and distinct C-terminus, as compared to isoform 1. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AF044323.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025094 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## gene product(s) localized to mito. :: reported by MitoCarta ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-71 BX537557.1 1-71 72-182 DB094258.1 73-183 183-893 BX537557.1 183-893 894-1736 AF044323.1 328-1170 1737-3354 BC078161.1 2388-4005 3355-6450 AL133353.6 57310-60405 c FEATURES Location/Qualifiers source 1..6450 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="10" /map="10q24" gene 1..6450 /gene="COX15" /gene_synonym="CEMCOX2" /note="cytochrome c oxidase assembly homolog 15 (yeast)" /db_xref="GeneID:1355" /db_xref="HGNC:2263" /db_xref="HPRD:04707" /db_xref="MIM:603646" exon 1..707 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" variation 175 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="g" /db_xref="dbSNP:2231674" variation 183 /gene="COX15" /gene_synonym="CEMCOX2" /replace="c" /replace="t" /db_xref="dbSNP:2231675" misc_feature 387..389 /gene="COX15" /gene_synonym="CEMCOX2" /note="upstream in-frame stop codon" variation 525 /gene="COX15" /gene_synonym="CEMCOX2" /replace="c" /replace="g" /db_xref="dbSNP:2231676" variation 592 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="g" /db_xref="dbSNP:2231677" variation 595 /gene="COX15" /gene_synonym="CEMCOX2" /replace="g" /replace="t" /db_xref="dbSNP:2231678" CDS 618..1784 /gene="COX15" /gene_synonym="CEMCOX2" /note="isoform 2 is encoded by transcript variant 2; cytochrome c oxidase subunit 15; cytochrome c oxidase assembly protein COX15 homolog; COX15 homolog, cytochrome c oxidase assembly protein" /codon_start=1 /product="cytochrome c oxidase assembly protein COX15 homolog isoform 2" /protein_id="NP_004367.2" /db_xref="GI:17921987" /db_xref="CCDS:CCDS7481.1" /db_xref="GeneID:1355" /db_xref="HGNC:2263" /db_xref="HPRD:04707" /db_xref="MIM:603646" /translation="
MQRLLFPPLRALKGRQYLPLLAPRAAPRAQCDCIRRPLRPGQYSTISEVALQSGRGTVSLPSKAAERVVGRWLLVCSGTVAGAVILGGVTRLTESGLSMVDWHLIKEMKPPTSQEEWEAEFQRYQQFPEFKILNHDMTLTEFKFIWYMEYSHRMWGRLVGLVYILPAAYFWRKGWLSRGMKGRVLALCGLVCFQGLLGWYMVKSGLEEKSDSHDIPRVSQYRLAAHLGSALVLYCASLWTSLSLLLPPHKLPETHQLLQLRRFAHGTAGLVFLTALSGAFVAGLDAGLVYNSFPKMGESWIPEDLFTFSPILRNVFENPTMVQFDHRILGITSVTAITVLYFLSRRIPLPRRTKMAAVTLLALAYTQGPVLFNFTFKISDLDEGIRNI
" misc_feature 813..1718 /gene="COX15" /gene_synonym="CEMCOX2" /note="Cytochrome oxidase assembly protein; Region: COX15-CtaA; cl15852" /db_xref="CDD:210252" misc_feature 816..1718 /gene="COX15" /gene_synonym="CEMCOX2" /note="Uncharacterized protein required for cytochrome oxidase assembly [Posttranslational modification, protein turnover, chaperones]; Region: CtaA; COG1612" /db_xref="CDD:31800" misc_feature 819..881 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" misc_feature 1077..1130 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" misc_feature 1167..1229 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" misc_feature 1296..1358 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" misc_feature 1422..1484 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" misc_feature 1587..1649 /gene="COX15" /gene_synonym="CEMCOX2" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q7KZN9.1); transmembrane region" exon 708..889 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" STS 743..874 /gene="COX15" /gene_synonym="CEMCOX2" /standard_name="A008T04" /db_xref="UniSTS:17407" exon 890..1012 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" exon 1013..1199 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" variation 1165 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="g" /db_xref="dbSNP:35483721" exon 1200..1367 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" variation 1281 /gene="COX15" /gene_synonym="CEMCOX2" /replace="c" /replace="t" /db_xref="dbSNP:2231682" exon 1368..1449 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" exon 1450..1604 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" exon 1605..1718 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" exon 1719..6450 /gene="COX15" /gene_synonym="CEMCOX2" /inference="alignment:Splign:1.39.8" variation 1737 /gene="COX15" /gene_synonym="CEMCOX2" /replace="c" /replace="t" /db_xref="dbSNP:2231687" variation 2701 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="g" /db_xref="dbSNP:1802213" STS 3045..3220 /gene="COX15" /gene_synonym="CEMCOX2" /standard_name="RH44559" /db_xref="UniSTS:58606" variation 3079 /gene="COX15" /gene_synonym="CEMCOX2" /replace="g" /replace="t" /db_xref="dbSNP:12416" variation 3260 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="g" /db_xref="dbSNP:1128642" polyA_signal 3330..3335 /gene="COX15" /gene_synonym="CEMCOX2" polyA_site 3354 /gene="COX15" /gene_synonym="CEMCOX2" variation 5052 /gene="COX15" /gene_synonym="CEMCOX2" /replace="a" /replace="c" /db_xref="dbSNP:1056844" STS 6274..6440 /gene="COX15" /gene_synonym="CEMCOX2" /standard_name="RH65628" /db_xref="UniSTS:73963" ORIGIN
cacaaggtcgcagggccgttatgaggggaccccgggactcgaaccttggctccacagctgagccattctcgctacctgcccctcgtcacgccctccgtttccacacctttaacgcctcaaagatagaaggtgccgcccaaggggctggaaggagctgaggaaacgactccagaagaaatcaccactgactacgactcccgccggcccgccccggggagccttcggccgaccgtcccctcccccgccaccttccgcaccggccttcccggacggtatccgcgctcgttttcgctcagaggaggccccctgccttttcatgctccacgcgttcctccctcgtgcgcctgcagtttccacttggaatttgggctccggcgcgcaccagctaagaagcgcgtcaacagctgcgcgcgcccgtgcgcgcgtccccgacacctacgccccagcagcccccgcgaaagcggagtcgcaacgcaggcgcacttctgttcgctccggtccccagagaaggcggggctcccgctgcccgacccggaagtgcttctcttttccttggcggaggagggagaccacagagccctgggttgtggaagaggtggctgttccctgtcatcagtatgcagcgattgctctttccgccgttgagggccttgaaggggaggcagtatctgccgctcctggctcctagggcagcgcctagagcacagtgtgattgcatcaggcgccctttgaggccagggcaatacagcaccatctctgaagtagctttgcaatctggaaggggtacagtgtcccttccctcaaaggctgctgagcgggtggtgggccgatggctcctggtctgcagtggaacagtggctggagcagttattcttggtggagtaactaggttgacagagtctggcctctcgatggtagattggcatttaataaaggagatgaagccacctacaagccaagaggaatgggaagcagaattccaaagataccagcaatttccagaatttaaaatcttgaatcatgatatgacactgacagaattcaagttcatctggtacatggagtactcacaccgaatgtggggtcgccttgtaggccttgtgtacatcctgcctgctgcctacttttggagaaagggctggctcagccgtggcatgaaaggacgtgttcttgccctctgtggcctcgtctgcttccagggtctgttgggatggtatatggtgaaaagtggactagaagaaaaatcagactcccatgacatccctcgggtcagtcagtaccgccttgctgcccacctgggatcagccctggttctttattgtgccagcttgtggacctcactgtcactgctactccctccgcacaagttgcctgaaacccaccaactcctacagttgagacgatttgctcatggaacagcaggtctggtgttccttacggccctctcaggggcttttgtggcagggctagatgctgggcttgtttataactcctttcccaaaatgggagaatcctggatcccggaggacctctttaccttctcccccatcctgaggaatgtttttgagaatcccaccatggtgcagtttgatcaccggattctgggaatcacttcagtcactgccattacagtgctctacttcctctctcggagaattccccttcctagaaggaccaagatggcagcagtgactctgctggctttggcgtatacacagggccctgtcttattcaactttacttttaaaatcagtgatttggatgaaggcatcagaaacatctgatttgaggatggagcaacccaatattgctaatataatagatgacagtggcaactgaaaacagtcccagaatgaccccatcgagatgaaattaaacagattagaaatgtaacatactcatttaaattaaataagttgtataagtttgggctgaagaaacctggccttatatcatttcatataaaaaagacgggattttagttgtcctcaggttcaatatgaaccaagtagtattcatgttgttattatatgataacagaaaaattagtggtacttcaggttttatcagtagaagtgtcacagccatagtcaaaatacccctaacatactgcatttcactctgggtaccaaatttaagcaagatattgatggccactaagtgtgtatccagaagaagagatcagaatgatgagtccagaacccctgtcacacagggaataggtgaaggaactagggatatttaactggagcagagaacatctggagagagagcaagattcctgtccttgagaagttgaagccgtctcatgcagaagagggaatgagcttccattatgctgcagagctggcagcaatggatgaaagttgcaggaagttagttttagttctgtagaaggcaagagtagggtagaccaaatcaaatgctcactggggtcaggctgatggagacagtaacactggcgagcaggtgccccagctcggactatactgctgagttctggtctgttgctgccactctacaggtccagggttgttagatcttctgggtttttgttttgctttttgaaataaggaaaataagcttatcttaagtttatttttccttggatatacctagattccatacagtgacaatacaaatacaaaggaagaacatctggatttcatccttgacctcatttacaaagcaaaaagagatgctggattcagatataaatgtttaattttgcagtgtttaagtcagcaaatcttctgttttttaaaaataagccacatatctagatttttctgtgaaagctctcaattaagtgttgggaactaatttcaagattttaaaaaatgttatgcaggcttaacgtgtctgagagccataaatgacctaacgtttcccgttagtctctgaactaggtgatctcagttctctttcaactccagtactctgtaagtttctgtgacctgtagtgtaccattctcaggtggtgatatggtttggatgttttgtcccctccaaatctcatgttcaaagtgtgacattcagtgttagaggtgggcctagtaggaggtatttgggtcatgggggcggatcccttatgtatgactttgtgccatccccatagtaatgagtgagttctcactctggttgtttatgcaagagctggttgtttaaaagagcctggaacttcctcctctctcgcttgctctctctcaccatgtgacacactggctccccttcaccttctgccatgattgtaagcttcgtgaggccctcaccagaagcagatgccagcgccatgcttcctatacagttctatgcagaacagtgagccaaataaacctcttttctttctaaaaattgtcagtatttccttatagcaatgcaagccgactaacacaggtgattcttagcaaaacagtttgtcaatttttcataaatgctggaccctggctgggcttatgctattgcctagaagagattcccaacttctctcttatttgaatcttagaaaaatcccaaagcccaagcctcatctaagaccaattaagtcacaatccctggaggaagtaaaaggcatatttttaaagttccccaggtgattccaatgtgcagacaagtctagggaccactggcttaggtcctaatagcctagttaccttagaaagttctgactagcttattcccattcccttctaatttccaccccaccttatcatttgatctgctatgttgctcctattagtatgttagtaggatatggtctcttctggatagaatccttcaaagaaagggaactgtagttcctgaggcaggttcccacaccatcctctcctgatcctcaaacccaggttgtccttagttagtaactgagtcagcagagggcagtatgacccaacccaaagaaccatatattaatgcttctacagttgcctccaaggaagtagcaactcatgagtaagttaaggtttcagatgttttacttcatttttcttttattacagatgatgagtacatttggaaaaacaactggttgcatttagctatataactgtattatatctatgagcttctggtgaatgattatcttagggttttttttgtatttatgttattcccagcactcccagacacatatcaaatattgaattagtgaatgcatgaatggaaaatggataattacagattgatgttccaaatacctttttccaaaaaaacaagtcatcacatacctataggattaaatagatttcccttaatattttcaaaggtctctctgcacttacgtccattgtttttaaaacatgaaggaaattaaaacacatggctttcttaatcagtcaacctagaattttttgtctgtaacttagactgacaaatactatctattgtagcaggggtaatgactagcaactccctaaagcaatgttggttgcagagatcaacactgataatcatgattttaggataaccagtttatctacagctacccttgtggtcctgggatgaatggtgggttatatatcagcatatgtaacacatatacccatgtccctgcataagggagaatgcatcacctctctaacatgcatcacacattttcctcaacactgacctaaaatgtttgtcagtgagaattttaagaattcaaaattcaacaaaattattgtttaatgtgaagcagtagaaaaaacagagtcttaacaactccccaaagcaatgtaatacaggcagcctttggttttttaaagtgtagatcataataaaaagatgtctttcactacactccgcagaggccattgatcaaggtagaaataaagggggagtacatggcatgtacttcaggacttcaactaaagggtaattgtggaatgagaatttcaaatacaacatagtaactgaaacactagaaaccaaagtatgtgtctgggatccctgcttgcagaaaaacatttatgaagctagtaaggggcgtcttcaccagcagcaggccaaatgccggcaagtgctctgtaggaggggccacttaggaaagtaccagggctgccttggagtggagaaggaggagtggccaccagagggtatacaagtggttgccctttaaaagaagaggctcaggagcagacatgtctttatgctagcctgaagtcatgcatgtgtggctatacatagcctgtgattcagaagacttttcaactttggttttcataaaaatggcaagcaatgatggattacattttaaaagtgaaagcccttgtagtatgagtaatgattcagttttactaataaaaggatctccgtattgctcagattttcagagaaacaaaatggtcaactggtgtgttattccttcctcgtccctctgataacggtactgacaaactggaaaataatgaaatattagagcaaaagagaaatgtgtaataacacaagagaagtctattaggatataaggaagataagtagacagagcaggcttaaaatgaagcttgaacaagccatctgcagaaacagaaaacagggtagatgggacacccaaacagggtgccacagctttccaacttagatccaggttatgagagaatgagccaagaacacaacctaaaagttttcaatttgaggtatattcactgttgctattctatagtattaatcaaaatattattgactaataatcctgttattattaatcacaacttttggttttgagtcttagttttttaacagcaatattttttgtaacaccaggaaaatcctcacaagttattgccccaggggctggaatctggagctagcgtccctaagagactaatatgggagaatttgaaacatctgctatttctaccataattcttattcccaatcaacattacaccacataccacagcaaaaaggacaattagatactagttttgaattaatttgaaaagtttaaagacaacaaaaagaaacagccctctgtttctgtaacagagtctggaaactgcccaagaattacaacgaagttctttaatgaggtagatgtaataggcatttataccttcatctaggctgtagtcatctaatgaattgcttggatgttgtagtaaaggaaattgtataaaattgttttaaaaagatgtataaaatttaaaagtacgaaaagaaatacaggaacaagaatagatgtagtgaaaacttggcactatttctgacaaagtatttttttcaaagtttattcctaaatgtgagcaaagcagtcataaatgaatgtcagaagcagttgtaaagatggggcatggttagttgtggccagctgttttataaaaaatagattctgtttatacttgcagaaagattctgttaatgagcatttcattgtagctgacaaagtagttgggctaggaggccagtcactatgactttgcacatattacaactgctctaggcctcagttttatcacccatataaatcaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:1355 -> Molecular function: GO:0004129 [cytochrome-c oxidase activity] evidence: IGI GeneID:1355 -> Molecular function: GO:0004129 [cytochrome-c oxidase activity] evidence: TAS GeneID:1355 -> Molecular function: GO:0016627 [oxidoreductase activity, acting on the CH-CH group of donors] evidence: IEA GeneID:1355 -> Biological process: GO:0006123 [mitochondrial electron transport, cytochrome c to oxygen] evidence: IC GeneID:1355 -> Biological process: GO:0006778 [porphyrin-containing compound metabolic process] evidence: TAS GeneID:1355 -> Biological process: GO:0006783 [heme biosynthetic process] evidence: TAS GeneID:1355 -> Biological process: GO:0006784 [heme a biosynthetic process] evidence: IEA GeneID:1355 -> Biological process: GO:0006784 [heme a biosynthetic process] evidence: IGI GeneID:1355 -> Biological process: GO:0007585 [respiratory gaseous exchange] evidence: TAS GeneID:1355 -> Biological process: GO:0008535 [respiratory chain complex IV assembly] evidence: IMP GeneID:1355 -> Biological process: GO:0044281 [small molecule metabolic process] evidence: TAS GeneID:1355 -> Biological process: GO:0045333 [cellular respiration] evidence: IC GeneID:1355 -> Biological process: GO:0055114 [oxidation-reduction process] evidence: TAS GeneID:1355 -> Cellular component: GO:0005739 [mitochondrion] evidence: IDA GeneID:1355 -> Cellular component: GO:0005743 [mitochondrial inner membrane] evidence: TAS GeneID:1355 -> Cellular component: GO:0005746 [mitochondrial respiratory chain] evidence: TAS GeneID:1355 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
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