Felis catus (domestic cat): 101088122 Help Entry 101088122         CDS       T02385                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca01524   Platinum drug resistance fca04115   p53 signaling pathway fca04210   Apoptosis fca04215   Apoptosis - multiple species fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05132   Salmonella infection fca05134   Legionellosis fca05145   Toxoplasmosis fca05152   Tuberculosis fca05160   Hepatitis C fca05161   Hepatitis B fca05162   Measles fca05163   Human cytomegalovirus infection fca05164   Influenza A fca05167   Kaposi sarcoma-associated herpesvirus infection fca05168   Herpes simplex virus 1 infection fca05169   Epstein-Barr virus infection fca05170   Human immunodeficiency virus 1 infection fca05200   Pathways in cancer fca05210   Colorectal cancer fca05222   Small cell lung cancer fca05416   Viral myocarditis fca05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101088122  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     101088122    04215 Apoptosis - multiple species     101088122    04115 p53 signaling pathway     101088122  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101088122   09162 Cancer: specific types    05210 Colorectal cancer     101088122    05222 Small cell lung cancer     101088122   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     101088122    05161 Hepatitis B     101088122    05160 Hepatitis C     101088122    05164 Influenza A     101088122    05162 Measles     101088122    05168 Herpes simplex virus 1 infection     101088122    05163 Human cytomegalovirus infection     101088122    05167 Kaposi sarcoma-associated herpesvirus infection     101088122    05169 Epstein-Barr virus infection     101088122   09171 Infectious disease: bacterial    05132 Salmonella infection     101088122    05134 Legionellosis     101088122    05152 Tuberculosis     101088122   09174 Infectious disease: parasitic    05145 Toxoplasmosis     101088122   09164 Neurodegenerative disease    05010 Alzheimer disease     101088122    05012 Parkinson disease     101088122    05014 Amyotrophic lateral sclerosis     101088122    05016 Huntington disease     101088122    05017 Spinocerebellar ataxia     101088122    05020 Prion disease     101088122    05022 Pathways of neurodegeneration - multiple diseases     101088122   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     101088122    05416 Viral myocarditis     101088122   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101088122   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     101088122 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Motif Other DBs NCBI-GeneID:  101088122 NCBI-ProteinID:  XP_011286768 LinkDB All DBs Position D4:complement(82413489..82414759) Genome browser AA seq 93 aa AA seqDB search MGDVEQGKIFVQKCAQHHDAEKGGKHKTGPNLHGLFGWKAGQTPGFSYMDANQNKGTSWG EETLTEYLENPEKYIPETKMIFAGIKKARERAD NT seq 282 nt NT seq  +upstreamnt  +downstreamnt atgggtgacgttgagcagggcaagatttttgttcagaagtgtgcccagcaccatgacgcg gaaaagggaggcaagcacaagactgggccaaatctccatggtttatttgggtggaaggca ggtcaaacccctggattttcttacatggatgccaaccagaacaaaggcacctcctgggga gaggagacactgacggagtatttggagaatcccgagaagtacatccctgaaacaaaaatg atctttgctggcatcaagaaggcaagggaaagagcagactag

Felis catus (domestic cat): 101094614 Help Entry 101094614         CDS       T02385                                  Name (RefSeq) cytochrome c, testis-specific-like   KO K08738   cytochrome c Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca01524   Platinum drug resistance fca04115   p53 signaling pathway fca04210   Apoptosis fca04215   Apoptosis - multiple species fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05132   Salmonella infection fca05134   Legionellosis fca05145   Toxoplasmosis fca05152   Tuberculosis fca05160   Hepatitis C fca05161   Hepatitis B fca05162   Measles fca05163   Human cytomegalovirus infection fca05164   Influenza A fca05167   Kaposi sarcoma-associated herpesvirus infection fca05168   Herpes simplex virus 1 infection fca05169   Epstein-Barr virus infection fca05170   Human immunodeficiency virus 1 infection fca05200   Pathways in cancer fca05210   Colorectal cancer fca05222   Small cell lung cancer fca05416   Viral myocarditis fca05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101094614  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     101094614    04215 Apoptosis - multiple species     101094614    04115 p53 signaling pathway     101094614  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101094614   09162 Cancer: specific types    05210 Colorectal cancer     101094614    05222 Small cell lung cancer     101094614   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     101094614    05161 Hepatitis B     101094614    05160 Hepatitis C     101094614    05164 Influenza A     101094614    05162 Measles     101094614    05168 Herpes simplex virus 1 infection     101094614    05163 Human cytomegalovirus infection     101094614    05167 Kaposi sarcoma-associated herpesvirus infection     101094614    05169 Epstein-Barr virus infection     101094614   09171 Infectious disease: bacterial    05132 Salmonella infection     101094614    05134 Legionellosis     101094614    05152 Tuberculosis     101094614   09174 Infectious disease: parasitic    05145 Toxoplasmosis     101094614   09164 Neurodegenerative disease    05010 Alzheimer disease     101094614    05012 Parkinson disease     101094614    05014 Amyotrophic lateral sclerosis     101094614    05016 Huntington disease     101094614    05017 Spinocerebellar ataxia     101094614    05020 Prion disease     101094614    05022 Pathways of neurodegeneration - multiple diseases     101094614   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     101094614    05416 Viral myocarditis     101094614   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101094614   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     101094614 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  101094614 NCBI-ProteinID:  XP_003990999 LinkDB All DBs Position C1:complement(168719323..168745960) Genome browser AA seq 132 aa AA seqDB search MRLAEKEWAPQSCDPSAHWLRADADRRGDAKAGEKIFIQKCAQCHTVEKGGKHKTGPNLW GLSGPGRKTGQAPGFSFSDANKNRGIIWGEETLIEYLENPKEYIPGTKMVFAGLKKSERD DLIQYLKQATSS NT seq 399 nt NT seq  +upstreamnt  +downstreamnt atgagactggctgagaaggagtgggcaccgcagtcttgtgatccgagcgctcactggtta cgggccgatgcagatagaaggggagatgctaaagcaggtgagaagatctttattcagaaa tgtgctcagtgccacacagtggaaaaaggtggaaaacacaagactggtccaaatctctgg ggcctttctggccctggacgaaaaacaggacaagcaccaggattttctttttccgatgct aacaaaaacagaggtattatctggggagaggaaactctgatagaatatttagagaaccca aaggaatatatccctggaactaaaatggtctttgctggtcttaaaaagagtgagagagat gatctcattcagtatttgaaacaggcaacatcttcatga

Felis catus (domestic cat): 101098213 Help Entry 101098213         CDS       T02385                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca01524   Platinum drug resistance fca04115   p53 signaling pathway fca04210   Apoptosis fca04215   Apoptosis - multiple species fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05132   Salmonella infection fca05134   Legionellosis fca05145   Toxoplasmosis fca05152   Tuberculosis fca05160   Hepatitis C fca05161   Hepatitis B fca05162   Measles fca05163   Human cytomegalovirus infection fca05164   Influenza A fca05167   Kaposi sarcoma-associated herpesvirus infection fca05168   Herpes simplex virus 1 infection fca05169   Epstein-Barr virus infection fca05170   Human immunodeficiency virus 1 infection fca05200   Pathways in cancer fca05210   Colorectal cancer fca05222   Small cell lung cancer fca05416   Viral myocarditis fca05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101098213  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     101098213    04215 Apoptosis - multiple species     101098213    04115 p53 signaling pathway     101098213  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101098213   09162 Cancer: specific types    05210 Colorectal cancer     101098213    05222 Small cell lung cancer     101098213   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     101098213    05161 Hepatitis B     101098213    05160 Hepatitis C     101098213    05164 Influenza A     101098213    05162 Measles     101098213    05168 Herpes simplex virus 1 infection     101098213    05163 Human cytomegalovirus infection     101098213    05167 Kaposi sarcoma-associated herpesvirus infection     101098213    05169 Epstein-Barr virus infection     101098213   09171 Infectious disease: bacterial    05132 Salmonella infection     101098213    05134 Legionellosis     101098213    05152 Tuberculosis     101098213   09174 Infectious disease: parasitic    05145 Toxoplasmosis     101098213   09164 Neurodegenerative disease    05010 Alzheimer disease     101098213    05012 Parkinson disease     101098213    05014 Amyotrophic lateral sclerosis     101098213    05016 Huntington disease     101098213    05017 Spinocerebellar ataxia     101098213    05020 Prion disease     101098213    05022 Pathways of neurodegeneration - multiple diseases     101098213   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     101098213    05416 Viral myocarditis     101098213   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101098213   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     101098213 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  101098213 NCBI-ProteinID:  XP_006929319 UniProt:  M3X7H4 LinkDB All DBs Position A2:complement(118772069..118774574) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKAGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaatctccacggtttatttgggcgaaag acaggccaagcccctgggttttcttacacggatgccaacaagaacaaaggcatcacctgg ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaaggcaggggaaagagcagacttgatagcttatctcaaa aaagctactaaggagtaa

Felis catus (domestic cat): 101100947 Help Entry 101100947         CDS       T02385                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism fca  Felis catus (domestic cat) Pathway fca00190   Oxidative phosphorylation fca01100   Metabolic pathways fca01524   Platinum drug resistance fca04115   p53 signaling pathway fca04210   Apoptosis fca04215   Apoptosis - multiple species fca04932   Non-alcoholic fatty liver disease fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05132   Salmonella infection fca05134   Legionellosis fca05145   Toxoplasmosis fca05152   Tuberculosis fca05160   Hepatitis C fca05161   Hepatitis B fca05162   Measles fca05163   Human cytomegalovirus infection fca05164   Influenza A fca05167   Kaposi sarcoma-associated herpesvirus infection fca05168   Herpes simplex virus 1 infection fca05169   Epstein-Barr virus infection fca05170   Human immunodeficiency virus 1 infection fca05200   Pathways in cancer fca05210   Colorectal cancer fca05222   Small cell lung cancer fca05416   Viral myocarditis fca05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:fca00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     101100947  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     101100947    04215 Apoptosis - multiple species     101100947    04115 p53 signaling pathway     101100947  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     101100947   09162 Cancer: specific types    05210 Colorectal cancer     101100947    05222 Small cell lung cancer     101100947   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     101100947    05161 Hepatitis B     101100947    05160 Hepatitis C     101100947    05164 Influenza A     101100947    05162 Measles     101100947    05168 Herpes simplex virus 1 infection     101100947    05163 Human cytomegalovirus infection     101100947    05167 Kaposi sarcoma-associated herpesvirus infection     101100947    05169 Epstein-Barr virus infection     101100947   09171 Infectious disease: bacterial    05132 Salmonella infection     101100947    05134 Legionellosis     101100947    05152 Tuberculosis     101100947   09174 Infectious disease: parasitic    05145 Toxoplasmosis     101100947   09164 Neurodegenerative disease    05010 Alzheimer disease     101100947    05012 Parkinson disease     101100947    05014 Amyotrophic lateral sclerosis     101100947    05016 Huntington disease     101100947    05017 Spinocerebellar ataxia     101100947    05020 Prion disease     101100947    05022 Pathways of neurodegeneration - multiple diseases     101100947   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     101100947    05416 Viral myocarditis     101100947   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     101100947   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     101100947 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  101100947 NCBI-ProteinID:  XP_011290006 UniProt:  M3X7H4 LinkDB All DBs Position X:complement(43153840..43155056) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKAGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaatctccacggtttatttgggcgaaag acaggccaagcccctgggttttcttacacggatgccaacaagaacaaaggcatcacctgg ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaaggcaggggaaagagcagacttgatagcttatctcaaa aaagctactaaggagtaa

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