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 CCP_MauG Motif Other DBs NCBI-GeneID:  101098213 NCBI-ProteinID:  XP_006929319 Ensembl:  ENSFCAG00000036552 UniProt:  M3X7H4 LinkDB All DBs Position A2:complement(117139725..117142254) 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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