Canis lupus dingo (dingo): 112670591 Help Entry 112670591         CDS       T08371                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism clud  Canis lupus dingo (dingo) Pathway clud00190   Oxidative phosphorylation clud01100   Metabolic pathways clud01524   Platinum drug resistance clud04115   p53 signaling pathway clud04210   Apoptosis clud04215   Apoptosis - multiple species clud04932   Non-alcoholic fatty liver disease clud05010   Alzheimer disease clud05012   Parkinson disease clud05014   Amyotrophic lateral sclerosis clud05016   Huntington disease clud05017   Spinocerebellar ataxia clud05020   Prion disease clud05022   Pathways of neurodegeneration - multiple diseases clud05132   Salmonella infection clud05134   Legionellosis clud05145   Toxoplasmosis clud05152   Tuberculosis clud05160   Hepatitis C clud05161   Hepatitis B clud05162   Measles clud05163   Human cytomegalovirus infection clud05164   Influenza A clud05167   Kaposi sarcoma-associated herpesvirus infection clud05168   Herpes simplex virus 1 infection clud05169   Epstein-Barr virus infection clud05170   Human immunodeficiency virus 1 infection clud05200   Pathways in cancer clud05210   Colorectal cancer clud05222   Small cell lung cancer clud05416   Viral myocarditis clud05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:clud00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     112670591  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     112670591    04215 Apoptosis - multiple species     112670591    04115 p53 signaling pathway     112670591  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112670591   09162 Cancer: specific types    05210 Colorectal cancer     112670591    05222 Small cell lung cancer     112670591   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     112670591    05161 Hepatitis B     112670591    05160 Hepatitis C     112670591    05164 Influenza A     112670591    05162 Measles     112670591    05168 Herpes simplex virus 1 infection     112670591    05163 Human cytomegalovirus infection     112670591    05167 Kaposi sarcoma-associated herpesvirus infection     112670591    05169 Epstein-Barr virus infection     112670591   09171 Infectious disease: bacterial    05132 Salmonella infection     112670591    05134 Legionellosis     112670591    05152 Tuberculosis     112670591   09174 Infectious disease: parasitic    05145 Toxoplasmosis     112670591   09164 Neurodegenerative disease    05010 Alzheimer disease     112670591    05012 Parkinson disease     112670591    05014 Amyotrophic lateral sclerosis     112670591    05016 Huntington disease     112670591    05017 Spinocerebellar ataxia     112670591    05020 Prion disease     112670591    05022 Pathways of neurodegeneration - multiple diseases     112670591   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     112670591    05416 Viral myocarditis     112670591   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     112670591   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     112670591 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  112670591 NCBI-ProteinID:  XP_025320200 Ensembl:  ENSCAFG00020003401 LinkDB All DBs Position 14:complement(38451966..38454570) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcgcagtgccatact gtggaaaagggaggcaagcacaagactgggccaaacctccacggtttatttgggcggaag accggtcaggcccctggattttcttacacggatgccaacaagaacaaaggcatcacctgg ggagaggagaccctgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaagacaggggaaagagcagacttaatagcttatctcaaa aaagctactaaggagtaa

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