Felis catus (domestic cat): 101086703 Help Entry 101086703         CDS       T02385                                  Name (RefSeq) cytochrome b-c1 complex subunit 10   KO K00420   ubiquinol-cytochrome c reductase subunit 10 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101086703  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101086703   09159 Environmental adaptation    04714 Thermogenesis     101086703  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101086703   09164 Neurodegenerative disease    05010 Alzheimer disease     101086703    05012 Parkinson disease     101086703    05014 Amyotrophic lateral sclerosis     101086703    05016 Huntington disease     101086703    05020 Prion disease     101086703    05022 Pathways of neurodegeneration - multiple diseases     101086703   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101086703   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101086703 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UCR_6-4kD QCR10 Motif Other DBs NCBI-GeneID:  101086703 NCBI-ProteinID:  XP_003981660 Ensembl:  ENSFCAG00000002620 UniProt:  M3VYU3 LinkDB All DBs Position A2:complement(936175..938611) Genome browser AA seq 56 aa AA seqDB search MLSRFLGPRYRELARNWIPTAGMWGAVGAVGLVWATDWRLILDWVPYINGKFKKDD NT seq 171 nt NT seq  +upstreamnt  +downstreamnt atgctgagcaggttcctgggcccgcgctaccgcgagctggccagaaactggattcccaca gcaggcatgtggggcgccgtgggcgccgtggggctggtgtgggccacggattggcggctc attctggactgggtgccctacatcaacggcaagtttaagaaggacgattag

Felis catus (domestic cat): 101089499 Help Entry 101089499         CDS       T02385                                  Symbol UQCRC1 Name (RefSeq) cytochrome b-c1 complex subunit 1, mitochondrial isoform X2   KO K00414   ubiquinol-cytochrome c reductase core subunit 1 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101089499 (UQCRC1)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101089499 (UQCRC1)   09159 Environmental adaptation    04714 Thermogenesis     101089499 (UQCRC1)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101089499 (UQCRC1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101089499 (UQCRC1)    05012 Parkinson disease     101089499 (UQCRC1)    05014 Amyotrophic lateral sclerosis     101089499 (UQCRC1)    05016 Huntington disease     101089499 (UQCRC1)    05020 Prion disease     101089499 (UQCRC1)    05022 Pathways of neurodegeneration - multiple diseases     101089499 (UQCRC1)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101089499 (UQCRC1)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101089499 (UQCRC1)  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:fca01002]     101089499 (UQCRC1) Peptidases and inhibitors [BR:fca01002]  Metallo peptidases   Family M16: pitrilysin family    101089499 (UQCRC1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Peptidase_M16 Peptidase_M16_C Motif Other DBs NCBI-GeneID:  101089499 NCBI-ProteinID:  XP_003982215 Ensembl:  ENSFCAG00000002100 LinkDB All DBs Position A2:complement(17864016..17873056) Genome browser AA seq 480 aa AA seqDB search MAASAVCRAASAGTRVLLRTHRSPALLRSPALRTTATFAQALQSVPETQVSLLDNGLRVA SEQSSQPTCTVGVWIDVGSRYETEKNNGAGYFLEHLAFKGTKNRPGNALEKEVESMGAHL NAYSTREHTAYYIKALSKDLPKAVELLADIVQNCALEDSQIEKERDVILQELQENDACMR DVVFDYLHATAFQGTPLAQAVEGPSGNVRKLSRADLTEYVSRHYKAPRMVLAAAGGVEHR QLVDLAQKHFSSVSETYTEDAVPTLAPCRFTGSEIRHRDDALPLAHVAIAVEGPGWANPD NVALQVANAIIGHYDCTYGGGMHLSSPLAAVAVANKLCQSFQTFNICYADTGLLGAHFVC DRMKIDDMMFFLQGQWMRLCTSATESEVLRGKNILRNALVSHLDGTTPVCEDIGRSLLTY GRRIPLAEWESRIAEVDASVVRDVCSKYFYDQCPAVAGFGPIEQLPDYNRIRSGMFWLRF NT seq 1443 nt NT seq  +upstreamnt  +downstreamnt atggcggcttccgcagtttgccgggcggctagcgccgggactcgagtgctgcttcgcacc caccgctcgccggccctgctgaggtcgcctgccttgaggaccaccgccaccttcgctcaa gctctccagagcgtgccggagacacaggtcagcttgctggacaacgggctgagagtggcc tccgagcagtcctcccagcctacctgcacggtcggggtatggattgatgttggcagccgt tacgagactgagaagaacaacggggcaggttactttctggagcatctggctttcaaggga acaaaaaatcggcctggcaatgccttggagaaggaggtggagagcatgggggcccatctc aatgcctacagcacccgggagcacacagcatactacatcaaggcgctatccaaggacctg ccaaaagctgtggagctcctggccgacattgtgcagaactgtgccctagaagactcccag attgagaaggagcgtgatgtgatcctacaggagctgcaggagaatgatgcatgtatgcgg gacgtggtctttgactacctgcacgccacagcattccagggcacacctctagcccaggct gtggaggggcccagtgggaatgtcaggaagctatctcgtgcagacctgaccgagtatgtc agcaggcattacaaggcccctcgcatggtgctcgcagcagccggaggggtggagcaccgg cagctggtagatctcgcccagaagcacttcagcagcgtctctgagacatacacagaggac gctgtgcccactcttgctccatgccgcttcactggcagcgagatccgccaccgcgacgat gctctgccattggcccatgtggctattgcggtagaggggcctggctgggccaacccggac aacgtggccctccaagtagccaatgccatcattggccactatgactgcacttatggtggt ggcatgcacctgtccagcccactggctgcagtcgccgtggccaacaagctgtgccagagt ttccagaccttcaatatctgctacgcagacactgggttgctgggtgcacactttgtctgc gatcgcatgaaaatcgatgacatgatgttcttcctgcaaggccagtggatgcgcctgtgc accagtgccacagagagtgaggtgctccggggcaaaaacatcctccgaaatgccctggtg tctcatctggatggcaccactcctgtgtgtgaggacatcggacgtagtctcctgacctat ggccgccgcattcccctggctgagtgggaaagccggattgcggaagtggatgccagtgtg gtacgtgatgtctgctccaagtacttctatgatcagtgtccagcagtggctggatttggc cccattgagcagctcccagactacaaccggatccgtagcggcatgttctggctgcgtttc tag

Felis catus (domestic cat): 101090590 Help Entry 101090590         CDS       T02385                                  Name (RefSeq) cytochrome b-c1 complex subunit 7   KO K00417   ubiquinol-cytochrome c reductase subunit 7 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101090590  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101090590   09159 Environmental adaptation    04714 Thermogenesis     101090590  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101090590   09164 Neurodegenerative disease    05010 Alzheimer disease     101090590    05012 Parkinson disease     101090590    05014 Amyotrophic lateral sclerosis     101090590    05016 Huntington disease     101090590    05020 Prion disease     101090590    05022 Pathways of neurodegeneration - multiple diseases     101090590   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101090590   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101090590 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UCR_14kD Motif Other DBs NCBI-GeneID:  101090590 NCBI-ProteinID:  XP_004000046 Ensembl:  ENSFCAG00000026302 UniProt:  M3XB84 LinkDB All DBs Position F2:complement(42823926..42828357) Genome browser AA seq 111 aa AA seqDB search MASRPAVAASSRWLEGIRKWYYNAAGFNKLGLMRDDTIYENDDVKEAIRRLPENLYNDRM FRIKRALDLTMRHQILPKEQWTKYEEDKFYLEPYLKEVIRERKEREEWAKK NT seq 336 nt NT seq  +upstreamnt  +downstreamnt atggcgagccggcctgcggttgcagcatcaagtcggtggctggagggtattcgaaaatgg tattacaatgctgcagggttcaataaactgggactaatgcgagatgatacaatatatgag aatgacgatgtgaaagaggccataagaaggcttcctgagaacctttataatgacaggatg tttcgcattaagagagcactggacctgaccatgaggcaccagatcttgcctaaagagcag tggacaaaatatgaggaggataaattctaccttgaaccatatctgaaagaagttattcgg gaaagaaaagaaagagaagaatgggcaaagaaataa

Felis catus (domestic cat): 101094239 Help Entry 101094239         CDS       T02385                                  Symbol CYC1 Name (RefSeq) cytochrome c1, heme protein, mitochondrial   KO K00413   ubiquinol-cytochrome c reductase cytochrome c1 subunit Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00151   Cytochrome bc1 complex respiratory unit fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101094239 (CYC1)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101094239 (CYC1)   09159 Environmental adaptation    04714 Thermogenesis     101094239 (CYC1)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101094239 (CYC1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101094239 (CYC1)    05012 Parkinson disease     101094239 (CYC1)    05014 Amyotrophic lateral sclerosis     101094239 (CYC1)    05016 Huntington disease     101094239 (CYC1)    05020 Prion disease     101094239 (CYC1)    05022 Pathways of neurodegeneration - multiple diseases     101094239 (CYC1)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101094239 (CYC1)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101094239 (CYC1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C1 Cytochrome_CBB3 Motif Other DBs NCBI-GeneID:  101094239 NCBI-ProteinID:  XP_004000264 Ensembl:  ENSFCAG00000011545 UniProt:  M3WFA4 LinkDB All DBs Position F2:82778625..82781114 Genome browser AA seq 325 aa AA seqDB search MAAAAASLRGAVLGPRGAGLPGARARSLLCGARPCQLPLRTPQAVSLSSKAGLSRGRKVM LSALGMLAAGGAGLAVALHSAVSASDLELHPPSYPWSHRGFLSSLDHTSIRRGFQVYKQV CSSCHSMDYVAYRHLVGVCYTEDEAKALAEEVEVQDGPNEDGEMFMRPGKLSDYFPKPYP NPEAARAANNGALPPDLSYIVRARHGGEDYVFSLLTGYCEPPTGVSLREGLYFNPYFPGQ AIGMAPPIYTEVLEYDDGTPATMSQVAKDVCTFLRWASEPEHDHRKRMGLKMLMMMGLLL PLVYAMKRHKWSVLKSRKLAYRPPK NT seq 978 nt NT seq  +upstreamnt  +downstreamnt atggcggcggcggcggcttcgcttcgcggggcggtgctgggcccgcggggcgcggggctg ccgggcgcgcgggcccggagtttgctgtgcggcgcgcggccctgccagctcccgctgcgg acgccacaggcagtgtccttgtcgtcgaaggccggtctgtcccggggccggaaagtgatg ctctcagcgttgggcatgctggcggcagggggtgcagggctagccgtggctctgcattcg gccgtgagcgccagtgacctggagctgcacccccccagctatccgtggtcccaccgtggc ttcctgtcttccctggaccacaccagtatccggaggggtttccaggtgtataagcaggtg tgctcctcctgccacagcatggactacgtggcctaccgccacctggtgggtgtctgctac acagaagatgaagctaaggcgctcgcagaagaggtggaggttcaggacggccccaacgag gatggggagatgttcatgcggccagggaagctgtctgactacttccccaagccctacccc aaccctgaggccgctcgagcagccaacaacggagcactgccccctgacctcagctacatc gtgcgagctaggcacggtggtgaggactacgtcttctccctgctaaccggctactgtgag ccgcccaccggtgtgtcattgcgagaaggtctctatttcaacccctactttcctggccag gccatcggcatggctcctcccatctacactgaggtcttggagtatgacgatggcacccca gctaccatgtcccaggtagccaaggatgtgtgtaccttcctgcgctgggcatccgagcca gagcatgaccatcgcaaacgcatggggctcaagatgttgatgatgatgggcttgctattg cctctggtctatgccatgaagcggcataagtggtcagtcctgaagagccggaagctggcg tatcggccacccaagtga

Felis catus (domestic cat): 101094311 Help Entry 101094311         CDS       T02385                                  Name (RefSeq) cytochrome b-c1 complex subunit Rieske, mitochondrial   KO K00411   ubiquinol-cytochrome c reductase iron-sulfur subunit [EC:7.1.1.8] Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04148   Efferocytosis fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00151   Cytochrome bc1 complex respiratory unit fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101094311  09140 Cellular Processes   09141 Transport and catabolism    04148 Efferocytosis     101094311  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101094311   09159 Environmental adaptation    04714 Thermogenesis     101094311  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101094311   09164 Neurodegenerative disease    05010 Alzheimer disease     101094311    05012 Parkinson disease     101094311    05014 Amyotrophic lateral sclerosis     101094311    05016 Huntington disease     101094311    05020 Prion disease     101094311    05022 Pathways of neurodegeneration - multiple diseases     101094311   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101094311   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101094311 Enzymes [BR:fca01000]  7. Translocases   7.1  Catalysing the translocation of protons    7.1.1  Linked to oxidoreductase reactions     7.1.1.8  quinol---cytochrome-c reductase      101094311 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UCR_TM Ubiq-Cytc-red_N Rieske Motif Other DBs NCBI-GeneID:  101094311 NCBI-ProteinID:  XP_003998010 UniProt:  M3X4Y3 LinkDB All DBs Position E2:23201582..23207109 Genome browser AA seq 274 aa AA seqDB search MLSVAARSGPFAPVLSATSRGVAGALRPLVQASVPATSEPPMLDVKRPFLCRESLSGQAA SRPLVASVGLNVPASVRYSHTDIRVPDFSDYRRTEVLDGTKSSKESSEARKGFSYLITAT TSIGVAYAAKNVVSQFVSSMSASADVLAMSKIEIKLSDIPEGKNMAFKWRGKPLFVRHRT KKEIEQEAAVEVSQLRDPQHDLDRVKKPEWVILIGVCTHLGCVPIANAGDFGGYYCPCHG SHYDASGRIRKGPAPLNLEVPSYEFTGDDMVIVG NT seq 825 nt NT seq  +upstreamnt  +downstreamnt atgttgtcggtggccgcccgttcgggcccgttcgcgcccgtcctatcggccacgtcccgc ggggtggcgggcgcgttgcggcctctggtgcaggcttcagtgcccgccacctcggagccg ccaatgctggacgtgaagcggcccttcctgtgccgggagtcgctgagtggccaggccgcg agccggcctttggtcgcctccgtgggcctcaatgtccctgcttctgttcgttattcccac acagacatcagagtgcctgacttctctgactatcgacgcaccgaagtgttagatggtaca aagtcttcaaaagagagcagtgaggctagaaaaggtttctcctatttgataactgcaaca actagtataggtgttgcatatgctgccaagaatgtcgtctcccagtttgtttccagcatg agtgcttctgctgatgtgttggccatgtcgaaaatcgaaatcaagctatccgatattcca gaaggcaagaacatggctttcaaatggagaggaaaaccgctgtttgtgcgtcatagaacc aagaaggaaattgagcaggaagctgcagttgaagtgtcccagttgagggacccgcagcat gatttagatcgagtaaagaaacctgaatgggttatcctgataggtgtttgcactcatctt ggttgtgtacccattgcaaatgcaggagattttggtggttattactgcccttgccatggg tcacactatgatgcttctggcaggatcaggaaggggcctgcacctctcaatcttgaagtt ccctcatatgagttcaccggtgatgacatggtgattgttggttag

Felis catus (domestic cat): 101095032 Help Entry 101095032         CDS       T02385                                  Name (RefSeq) cytochrome b-c1 complex subunit 6, mitochondrial isoform X1   KO K00416   ubiquinol-cytochrome c reductase subunit 6 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101095032  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101095032   09159 Environmental adaptation    04714 Thermogenesis     101095032  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101095032   09164 Neurodegenerative disease    05010 Alzheimer disease     101095032    05012 Parkinson disease     101095032    05014 Amyotrophic lateral sclerosis     101095032    05016 Huntington disease     101095032    05020 Prion disease     101095032    05022 Pathways of neurodegeneration - multiple diseases     101095032   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101095032   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101095032 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UCR_hinge STX6_10_61_N Motif Other DBs NCBI-GeneID:  101095032 NCBI-ProteinID:  XP_003990099 UniProt:  A0A337SWK8 LinkDB All DBs Position C1:36772708..36780910 Genome browser AA seq 91 aa AA seqDB search MGLEDERKMLTGSGDPKEEEEEEEELVDPLTTVREQCEQLEKCVKARERLELCDERVSSR SKTEEDCTEELFDFLHARDHCVAHKLFNSLK NT seq 276 nt NT seq  +upstreamnt  +downstreamnt atggggctggaggacgagcgaaagatgctgactgggtccggagaccccaaagaggaggaa gaggaggaggaggaattagtggatcctctaacaacggtgagagagcaatgcgagcagctg gagaaatgtgtaaaggctcgggagcggctagagctctgtgatgagcgcgtatcctccagg tcaaagacagaggaggattgcacagaggagctctttgacttcctgcatgcaagggaccat tgtgtggcccacaaactctttaacagcttgaaataa

Felis catus (domestic cat): 101096871 Help Entry 101096871         CDS       T02385                                  Symbol UQCRQ Name (RefSeq) cytochrome b-c1 complex subunit 8   KO K00418   ubiquinol-cytochrome c reductase subunit 8 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101096871 (UQCRQ)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101096871 (UQCRQ)   09159 Environmental adaptation    04714 Thermogenesis     101096871 (UQCRQ)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101096871 (UQCRQ)   09164 Neurodegenerative disease    05010 Alzheimer disease     101096871 (UQCRQ)    05012 Parkinson disease     101096871 (UQCRQ)    05014 Amyotrophic lateral sclerosis     101096871 (UQCRQ)    05016 Huntington disease     101096871 (UQCRQ)    05020 Prion disease     101096871 (UQCRQ)    05022 Pathways of neurodegeneration - multiple diseases     101096871 (UQCRQ)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101096871 (UQCRQ)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101096871 (UQCRQ) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UcrQ Cyt_b-c1_8 Motif Other DBs NCBI-GeneID:  101096871 NCBI-ProteinID:  XP_003980807 Ensembl:  ENSFCAG00000024071 UniProt:  M3X026 LinkDB All DBs Position A1:109582058..109583394 Genome browser AA seq 82 aa AA seqDB search MGREFGHLTRMRHVITYSLSPFEQRAFPHYFSKGIPNVLRRTRACILRVLPPFVGFYLVY TWGTQEFEKSKRKNPAAYENDK NT seq 249 nt NT seq  +upstreamnt  +downstreamnt atgggccgcgagtttgggcatctgacgcggatgcggcatgtgatcacctacagcttgtca cccttcgagcagcgcgccttcccgcactacttcagcaagggcatccccaacgtgctgcgc cgcacgcgggcgtgcatccttcgcgtcctgccgccgtttgtagggttttatcttgtctat acctgggggacccaggagtttgagaaatccaagaggaagaatccggctgcttatgaaaat gacaaatga

Felis catus (domestic cat): 101101684 Help Entry 101101684         CDS       T02385                                  Symbol UQCRC2 Name (RefSeq) cytochrome b-c1 complex subunit 2, mitochondrial   KO K00415   ubiquinol-cytochrome c reductase core subunit 2 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101101684 (UQCRC2)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     101101684 (UQCRC2)   09159 Environmental adaptation    04714 Thermogenesis     101101684 (UQCRC2)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101101684 (UQCRC2)   09164 Neurodegenerative disease    05010 Alzheimer disease     101101684 (UQCRC2)    05012 Parkinson disease     101101684 (UQCRC2)    05014 Amyotrophic lateral sclerosis     101101684 (UQCRC2)    05016 Huntington disease     101101684 (UQCRC2)    05020 Prion disease     101101684 (UQCRC2)    05022 Pathways of neurodegeneration - multiple diseases     101101684 (UQCRC2)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101101684 (UQCRC2)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101101684 (UQCRC2)  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:fca01002]     101101684 (UQCRC2) Peptidases and inhibitors [BR:fca01002]  Metallo peptidases   Family M16: pitrilysin family    101101684 (UQCRC2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Peptidase_M16 Peptidase_M16_C Motif Other DBs NCBI-GeneID:  101101684 NCBI-ProteinID:  XP_003998825 UniProt:  M3W8B7 LinkDB All DBs Position E3:complement(24037862..24069212) Genome browser AA seq 453 aa AA seqDB search MKLLSRAGSFSRFYSLKVAPKVKTTAAPAGVPPLPQDLEFTKLPNGLVIASLENYAPASR IGLFIKAGSRYEDSNNLGTSHLLRLASSLTTKGASSFKITRGIEAVGGKLSVTSTRENMA YTVECLRDDVDILMEFLLNVTTAPEFRRWEVADLQSQLRIDKAVAFQNPQARVIENLHAA AYRNALANSLYCPDYRIGKVTPDELHNYVQNHFTSARMALIGLGVSHPVLKQVAEQFLNM RGGLGLPSTKARYRGGEIREQNGDSLVHAALVAESATIGSAEANAFSVLQYVLGAGPHVK RGSNATSSLYQAVAKGVHQPFDVSAFNASYSDSGLFGIYTISQAAAAGDVIKAAYNQVKM IAQGNLSNTDVLAAKNKLKAGYLMSVESSEEFLDEVGSQALVAGSYTPPATVLQQIDSVA DTDVVNAAKKFVSGRKSMAASGNLGHTPFVDEL NT seq 1362 nt NT seq  +upstreamnt  +downstreamnt atgaagctgctaagcagagccgggtctttttcgaggttttattccctgaaagttgctccc aaagtgaagaccacagctgcccctgcaggagtgcctccgcttcctcaggaccttgagttt accaagttaccaaatggcttagtgattgcttctctggaaaactatgctcctgcatcaaga attggtttgttcattaaagcaggcagtagatatgaggactccaacaacttaggaacctct catttgcttcgtcttgcatccagtttgactacaaaaggagcttcatctttcaagataacc cgtggaattgaagcagttggtggtaaattaagtgtgacttcaaccagggaaaacatggcc tacaccgtggaatgtctgcgagatgatgttgatattctaatggagttcctgctcaatgtc accacagccccagaatttcgtcgttgggaagtagctgaccttcagtctcagctaaggatt gacaaagctgtggcttttcagaatccacaggctcgtgtcattgaaaatttgcatgctgca gcttaccgaaatgccttggctaattccctgtattgccctgattataggattggaaaagtg acaccagatgagttacataactatgtgcagaaccattttacaagtgcgagaatggctttg atcggacttggtgtgagtcatcctgttctaaagcaagttgctgaacagtttctcaacatg aggggtgggcttggtttacctagtacaaaggccagatatcgtggaggtgaaatccgagag cagaacggagacagcctcgtccatgctgcccttgtagcagaaagtgctacaataggaagt gcagaagcaaatgcatttagtgttctccagtatgtccttggtgctggaccacacgtcaag aggggcagcaatgctaccagctctctgtaccaggccgttgccaagggagttcaccagcca tttgatgtttccgcttttaatgccagttactcggattctggactctttgggatttatacc atttcacaggctgctgcagctggagatgttatcaaggctgcctataaccaagtaaaaatg attgctcaaggaaacctttccaatacagatgtcctagctgccaagaacaagctgaaagct ggctacctaatgtcagtggagtcttctgaggagttcctggatgaagtcgggtcccaggct ctggttgctggttcatacacaccaccagccacagtccttcagcagattgactccgtagca gacacagatgttgtaaatgctgcaaagaagtttgtttctggccggaagtcaatggcagca agtggaaatctggggcacacacctttcgttgatgagttgtaa

Felis catus (domestic cat): 105261050 Help Entry 105261050         CDS       T02385                                  Symbol UQCR10 Name (RefSeq) uncharacterized protein UQCR10 isoform X1   KO K00419   ubiquinol-cytochrome c reductase subunit 9 Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     105261050 (UQCR10)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     105261050 (UQCR10)   09159 Environmental adaptation    04714 Thermogenesis     105261050 (UQCR10)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     105261050 (UQCR10)   09164 Neurodegenerative disease    05010 Alzheimer disease     105261050 (UQCR10)    05012 Parkinson disease     105261050 (UQCR10)    05014 Amyotrophic lateral sclerosis     105261050 (UQCR10)    05016 Huntington disease     105261050 (UQCR10)    05020 Prion disease     105261050 (UQCR10)    05022 Pathways of neurodegeneration - multiple diseases     105261050 (UQCR10)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     105261050 (UQCR10)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     105261050 (UQCR10) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  UCR_UQCRX_QCR9 Motif Other DBs NCBI-GeneID:  105261050 NCBI-ProteinID:  XP_011286040 LinkDB All DBs Position D3:complement(23075627..23077796) Genome browser AA seq 134 aa AA seqDB search MGKKILPHYLGCPNLNPMRLFSPASHHLPLLFKTTSTEIQKNYISHKVLHAEGLWSPWSA AAQARAPQWRKMAAPTFTARLYSLLFRRTSTFALTIAVGALFFERAFDQGADAIYEHINE GKLWKHIKHKYENK NT seq 405 nt NT seq  +upstreamnt  +downstreamnt atgggtaaaaaaatcttaccgcactatctgggctgccctaatctgaatcctatgagactt ttctcccccgcaagccatcacttacctctgttgttcaaaacgacaagcactgagattcag aaaaactacatatcccataaagtgttgcacgccgagggcttgtggagcccatggtcggcc gcggcgcaggcgcgggctccacagtggagaaagatggcggccccgacgtttactgcgagg ttatactccctgttgttccgcaggacctccactttcgccctcaccatcgccgtgggcgct ttgttcttcgagcgcgccttcgaccaaggcgcggacgcgatctacgaacacatcaacgag gggaagctgtggaaacacatcaagcacaagtatgagaataagtag

Felis catus (domestic cat): 807931 Help Entry 807931            CDS       T02385                                  Symbol CYTB Name (RefSeq) cytochrome b   KO K00412   ubiquinol-cytochrome c reductase cytochrome b subunit Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca04260   Cardiac muscle contraction fca04714   Thermogenesis fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05208   Chemical carcinogenesis - reactive oxygen species fca05415   Diabetic cardiomyopathy Module fca_M00151   Cytochrome bc1 complex respiratory unit fca_M00152   Cytochrome bc1 complex Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     807931 (CYTB)  09150 Organismal Systems   09153 Circulatory system    04260 Cardiac muscle contraction     807931 (CYTB)   09159 Environmental adaptation    04714 Thermogenesis     807931 (CYTB)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     807931 (CYTB)   09164 Neurodegenerative disease    05010 Alzheimer disease     807931 (CYTB)    05012 Parkinson disease     807931 (CYTB)    05014 Amyotrophic lateral sclerosis     807931 (CYTB)    05016 Huntington disease     807931 (CYTB)    05020 Prion disease     807931 (CYTB)    05022 Pathways of neurodegeneration - multiple diseases     807931 (CYTB)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     807931 (CYTB)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     807931 (CYTB)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:fca03029]     807931 (CYTB) Mitochondrial biogenesis [BR:fca03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial DNA-encoded proteins    Mitochondrial respiratory chain complex III     807931 (CYTB) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrome_B Cytochrom_B_N_2 Cytochrom_B_C Motif Other DBs NCBI-GeneID:  807931 NCBI-ProteinID:  NP_008263 UniProt:  P48886 LinkDB All DBs Position MT:15038..16177 Genome browser AA seq 379 aa AA seqDB search MTNIRKSHPLIKIINHSFIDLPAPSNISAWWNFGSLLGVCLTLQILTGLFLAMHYTSDTM TAFSSVTHICRDVNYGWIIRYLHANGASMFFICLYMHVGRGMYYGSYTFSETWNIGIMLL FTVMATAFMGYVLPWGQMSFWGATVITNLLSAIPYIGTELVEWIWGGFSVDKATLTRFFG FHFILPFIISALAGVHLLFLHETGSNNPSGITSDSDKIPFHPYYTIKDILGLLVLVLTLM LLVLFSPDLLGDPDNYIPANPLNTPPHIKPEWYFLFAYAILRSIPNKLGGVLALVLSILV LAIIPILHTSKQRGMMFRPLSQCLFWLLVADLLTLTWIGGQPVEHPFITIGQLASILYFS TLLILMPISGIIENRLLKW NT seq 1140 nt NT seq  +upstreamnt  +downstreamnt atgaccaacattcgaaaatcacacccccttatcaaaattattaatcactcattcatcgat ctacccgccccatctaacatctcagcatgatgaaacttcggctcccttctaggagtctgc ctaaccttacaaatcctcaccggcctctttttggccatacactacacatcagacacaata accgccttttcatcagttacccacatctgtcgcgacgttaattatggctgaatcatccga tatttacacgccaacggagcttctatattctttatctgcctgtacatacatgtaggacgg ggaatatactacggctcctacaccttctcagagacatgaaacattggaatcatactatta tttacagtcatagccacagcttttatgggatacgtcctaccatgaggccaaatgtccttc tgaggagcaaccgtaatcactaacctcctgtcagcaattccatacatcgggactgaacta gtagaatgaatctgaggggggttctcagtagacaaagccaccctaacacgattctttggc ttccacttcattcttccattcattatctcagccttagcaggagtacacctcttattcctt catgaaacaggatctaacaacccctcaggaattacatccgattcagacaaaatcccattc cacccatactatacaatcaaagacatcctaggtcttctagtactagttttaacactcata ctactcgtcctattttcaccagacctgctaggagacccagacaactacatcccagccaac cctttaaatacccctccccatattaaacctgaatgatacttcctattcgcatacgcaatt ctccgatccatccctaacaaactagggggagtcctagccctagtactctccatcctagta ctagcaatcattccaatcctccacacctccaaacaacgaggaataatgtttcgaccacta agccaatgtctattctgactcctagtagcggatctcctaaccctaacatgaatcggtggc caacctgtagaacatccgttcatcaccatcgggcaactagcctccatcctatatttctca accctcctaatcctaatacccatctcaggcattattgaaaaccgtctactcaaatgaaga

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