Homo sapiens (human): 170712 Help Entry 170712            CDS       T01001                                  Symbol COX7B2 Name (RefSeq) cytochrome c oxidase subunit 7B2   KO K02271   cytochrome c oxidase subunit 7b Organism hsa  Homo sapiens (human) Pathway hsa00190   Oxidative phosphorylation hsa01100   Metabolic pathways hsa04260   Cardiac muscle contraction hsa04714   Thermogenesis hsa04932   Non-alcoholic fatty liver disease hsa05010   Alzheimer disease hsa05012   Parkinson disease hsa05014   Amyotrophic lateral sclerosis hsa05016   Huntington disease hsa05020   Prion disease hsa05022   Pathways of neurodegeneration - multiple diseases hsa05208   Chemical carcinogenesis - reactive oxygen species hsa05415   Diabetic cardiomyopathy Module hsa_M00154   Cytochrome c oxidase Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     170712 (COX7B2)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     170712 (COX7B2)   09159 Environmental adaptation    04714 Thermogenesis     170712 (COX7B2)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     170712 (COX7B2)   09164 Neurodegenerative disease    05010 Alzheimer disease     170712 (COX7B2)    05012 Parkinson disease     170712 (COX7B2)    05014 Amyotrophic lateral sclerosis     170712 (COX7B2)    05016 Huntington disease     170712 (COX7B2)    05020 Prion disease     170712 (COX7B2)    05022 Pathways of neurodegeneration - multiple diseases     170712 (COX7B2)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     170712 (COX7B2)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     170712 (COX7B2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  COX7B Deltameth_res Motif Other DBs NCBI-GeneID:  170712 NCBI-ProteinID:  NP_570972 OMIM:  609811 HGNC:  24381 Ensembl:  ENSG00000170516 UniProt:  Q8TF08 LinkDB All DBs Position 4:complement(46734827..46909245) Genome browser AA seq 81 aa AA seqDB search MMFPLARNALSSLKIQSILQSMARHSHVKHSPDFHDKYGNAVLASGTAFCVATWVFTATQ IGIEWNLSPVGRVTPKEWKHQ NT seq 246 nt NT seq  +upstreamnt  +downstreamnt atgatgtttcccttggccagaaatgcactaagcagtctcaagattcaaagcattctgcaa agcatggcaagacatagccatgtaaaacactcaccagattttcatgataaatatggtaat gctgtgctagccagtggaactgctttctgtgttgctacatgggtgtttacagccactcag attggaatagaatggaacctatcccctgttggcagagttaccccaaaagagtggaaacat cagtaa

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