Macaca mulatta (rhesus monkey): 698225 Help Entry 698225            CDS       T01028                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism mcc  Macaca mulatta (rhesus monkey) Pathway mcc00190   Oxidative phosphorylation mcc01100   Metabolic pathways mcc01524   Platinum drug resistance mcc04115   p53 signaling pathway mcc04210   Apoptosis mcc04215   Apoptosis - multiple species mcc04932   Non-alcoholic fatty liver disease mcc05010   Alzheimer disease mcc05012   Parkinson disease mcc05014   Amyotrophic lateral sclerosis mcc05016   Huntington disease mcc05017   Spinocerebellar ataxia mcc05020   Prion disease mcc05022   Pathways of neurodegeneration - multiple diseases mcc05132   Salmonella infection mcc05134   Legionellosis mcc05145   Toxoplasmosis mcc05152   Tuberculosis mcc05160   Hepatitis C mcc05161   Hepatitis B mcc05162   Measles mcc05163   Human cytomegalovirus infection mcc05164   Influenza A mcc05167   Kaposi sarcoma-associated herpesvirus infection mcc05168   Herpes simplex virus 1 infection mcc05169   Epstein-Barr virus infection mcc05170   Human immunodeficiency virus 1 infection mcc05200   Pathways in cancer mcc05210   Colorectal cancer mcc05222   Small cell lung cancer mcc05416   Viral myocarditis mcc05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:mcc00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     698225  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     698225    04215 Apoptosis - multiple species     698225    04115 p53 signaling pathway     698225  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     698225   09162 Cancer: specific types    05210 Colorectal cancer     698225    05222 Small cell lung cancer     698225   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     698225    05161 Hepatitis B     698225    05160 Hepatitis C     698225    05164 Influenza A     698225    05162 Measles     698225    05168 Herpes simplex virus 1 infection     698225    05163 Human cytomegalovirus infection     698225    05167 Kaposi sarcoma-associated herpesvirus infection     698225    05169 Epstein-Barr virus infection     698225   09171 Infectious disease: bacterial    05132 Salmonella infection     698225    05134 Legionellosis     698225    05152 Tuberculosis     698225   09174 Infectious disease: parasitic    05145 Toxoplasmosis     698225   09164 Neurodegenerative disease    05010 Alzheimer disease     698225    05012 Parkinson disease     698225    05014 Amyotrophic lateral sclerosis     698225    05016 Huntington disease     698225    05017 Spinocerebellar ataxia     698225    05020 Prion disease     698225    05022 Pathways of neurodegeneration - multiple diseases     698225   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     698225    05416 Viral myocarditis     698225   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     698225   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     698225 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  698225 NCBI-ProteinID:  XP_001088492 Ensembl:  ENSMMUG00000032513 LinkDB All DBs Position 18:20322407..20322767 Genome browser AA seq 105 aa AA seqDB search MGNVEKGKKIFTMKCSQCHTVEKGGKHKTGPNLHGLFGRKTVQAPGYSYTAANKNKGITW GEDTLMEYLENPKKCLPGTKMIFVGIKKKEERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtaatgttgagaaaggcaagaagatttttactatgaagtgttcccagtgccacacc gttgaaaagggaggcaaacacaagactgggccaaatctccatggtctcttcgggcggaag acagttcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtgcctccctggaacaaaa atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa aaagctactaatgagtaa

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