Macaca mulatta (rhesus monkey): 705449 Help Entry 705449            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     705449  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     705449    04215 Apoptosis - multiple species     705449    04115 p53 signaling pathway     705449  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     705449   09162 Cancer: specific types    05210 Colorectal cancer     705449    05222 Small cell lung cancer     705449   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     705449    05161 Hepatitis B     705449    05160 Hepatitis C     705449    05164 Influenza A     705449    05162 Measles     705449    05168 Herpes simplex virus 1 infection     705449    05163 Human cytomegalovirus infection     705449    05167 Kaposi sarcoma-associated herpesvirus infection     705449    05169 Epstein-Barr virus infection     705449   09171 Infectious disease: bacterial    05132 Salmonella infection     705449    05134 Legionellosis     705449    05152 Tuberculosis     705449   09174 Infectious disease: parasitic    05145 Toxoplasmosis     705449   09164 Neurodegenerative disease    05010 Alzheimer disease     705449    05012 Parkinson disease     705449    05014 Amyotrophic lateral sclerosis     705449    05016 Huntington disease     705449    05017 Spinocerebellar ataxia     705449    05020 Prion disease     705449    05022 Pathways of neurodegeneration - multiple diseases     705449   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     705449    05416 Viral myocarditis     705449   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     705449   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     705449 SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  705449 NCBI-ProteinID:  XP_014976173 LinkDB All DBs Position 17:1486775..1487868 Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVETGGKHKTGPNLHGLIGWKTGQAIGFSYIDTGKNKGITW GNDTLREYLENPRKYVPGTKMIFAGIKKTAERADLLAYLKKATSE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttgttcagaagtgtgcccagtgccacacc gtggaaacgggaggcaagcacaagactgggcctaatctccatggtctcatcgggtggaag acaggtcaggccattggattctcttacatagacaccggtaagaacaaaggcatcacctgg ggaaatgatacactgagggagtatttggagaatcccaggaagtacgttcctggaacaaaa atgatctttgccggcattaagaagacggcagaaagggcagacttgttagcttatctcaaa aaagctacaagtgagtaa

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