Capra hircus (goat): 106501717 Help Entry 106501717         CDS       T02910                                  Name (RefSeq) cytochrome c 2   KO K08738   cytochrome c Organism chx  Capra hircus (goat) Pathway chx00190   Oxidative phosphorylation chx01100   Metabolic pathways chx01524   Platinum drug resistance chx04115   p53 signaling pathway chx04210   Apoptosis chx04215   Apoptosis - multiple species chx04932   Non-alcoholic fatty liver disease chx05010   Alzheimer disease chx05012   Parkinson disease chx05014   Amyotrophic lateral sclerosis chx05016   Huntington disease chx05017   Spinocerebellar ataxia chx05020   Prion disease chx05022   Pathways of neurodegeneration - multiple diseases chx05132   Salmonella infection chx05134   Legionellosis chx05145   Toxoplasmosis chx05152   Tuberculosis chx05160   Hepatitis C chx05161   Hepatitis B chx05162   Measles chx05163   Human cytomegalovirus infection chx05164   Influenza A chx05167   Kaposi sarcoma-associated herpesvirus infection chx05168   Herpes simplex virus 1 infection chx05169   Epstein-Barr virus infection chx05170   Human immunodeficiency virus 1 infection chx05200   Pathways in cancer chx05210   Colorectal cancer chx05222   Small cell lung cancer chx05416   Viral myocarditis chx05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:chx00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     106501717  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     106501717    04215 Apoptosis - multiple species     106501717    04115 p53 signaling pathway     106501717  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     106501717   09162 Cancer: specific types    05210 Colorectal cancer     106501717    05222 Small cell lung cancer     106501717   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     106501717    05161 Hepatitis B     106501717    05160 Hepatitis C     106501717    05164 Influenza A     106501717    05162 Measles     106501717    05168 Herpes simplex virus 1 infection     106501717    05163 Human cytomegalovirus infection     106501717    05167 Kaposi sarcoma-associated herpesvirus infection     106501717    05169 Epstein-Barr virus infection     106501717   09171 Infectious disease: bacterial    05132 Salmonella infection     106501717    05134 Legionellosis     106501717    05152 Tuberculosis     106501717   09174 Infectious disease: parasitic    05145 Toxoplasmosis     106501717   09164 Neurodegenerative disease    05010 Alzheimer disease     106501717    05012 Parkinson disease     106501717    05014 Amyotrophic lateral sclerosis     106501717    05016 Huntington disease     106501717    05017 Spinocerebellar ataxia     106501717    05020 Prion disease     106501717    05022 Pathways of neurodegeneration - multiple diseases     106501717   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     106501717    05416 Viral myocarditis     106501717   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     106501717   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     106501717 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  106501717 NCBI-ProteinID:  XP_005675975 EnsemblRapid:  ENSCHIG00000026156 UniProt:  A0A452G617 LinkDB All DBs Position 2:complement(117517676..117538376) Genome browser AA seq 105 aa AA seqDB search MADAEAGKKIFIQKCAQCHTVEKGGKHKTGPNLWGLFGRKTGQAPGFSYTEANKNKGIIW GEQTLMEYLENPKKYIPGTKMIFAGLKKKSEREDLIEYLKQATSS NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atggcagatgctgaggcaggcaagaagatctttattcaaaaatgtgctcagtgccacaca gtggagaaaggtggaaaacacaagactggtccaaatctctggggcctttttggcagaaaa acaggacaagcgccaggattttcttataccgaggcaaacaaaaacaaaggcattatctgg ggagagcagactttgatggaatatttggagaacccaaagaaatatatccctggaactaaa atgatctttgctggtcttaaaaagaagagtgagagagaagatcttattgagtatttgaaa caggcaacatcttcatga

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