Rattus norvegicus (rat): 120099910 Help Entry 120099910         CDS       T01003                                  Name (RefSeq) cytochrome c, somatic-like   KO K08738   cytochrome c Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno01524   Platinum drug resistance rno04115   p53 signaling pathway rno04210   Apoptosis rno04215   Apoptosis - multiple species rno04932   Non-alcoholic fatty liver disease rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05017   Spinocerebellar ataxia rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05132   Salmonella infection rno05134   Legionellosis rno05145   Toxoplasmosis rno05152   Tuberculosis rno05160   Hepatitis C rno05161   Hepatitis B rno05162   Measles rno05163   Human cytomegalovirus infection rno05164   Influenza A rno05167   Kaposi sarcoma-associated herpesvirus infection rno05168   Herpes simplex virus 1 infection rno05169   Epstein-Barr virus infection rno05170   Human immunodeficiency virus 1 infection rno05200   Pathways in cancer rno05210   Colorectal cancer rno05222   Small cell lung cancer rno05416   Viral myocarditis rno05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     120099910  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     120099910    04215 Apoptosis - multiple species     120099910    04115 p53 signaling pathway     120099910  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     120099910   09162 Cancer: specific types    05210 Colorectal cancer     120099910    05222 Small cell lung cancer     120099910   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     120099910    05161 Hepatitis B     120099910    05160 Hepatitis C     120099910    05164 Influenza A     120099910    05162 Measles     120099910    05168 Herpes simplex virus 1 infection     120099910    05163 Human cytomegalovirus infection     120099910    05167 Kaposi sarcoma-associated herpesvirus infection     120099910    05169 Epstein-Barr virus infection     120099910   09171 Infectious disease: bacterial    05132 Salmonella infection     120099910    05134 Legionellosis     120099910    05152 Tuberculosis     120099910   09174 Infectious disease: parasitic    05145 Toxoplasmosis     120099910   09164 Neurodegenerative disease    05010 Alzheimer disease     120099910    05012 Parkinson disease     120099910    05014 Amyotrophic lateral sclerosis     120099910    05016 Huntington disease     120099910    05017 Spinocerebellar ataxia     120099910    05020 Prion disease     120099910    05022 Pathways of neurodegeneration - multiple diseases     120099910   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     120099910    05416 Viral myocarditis     120099910   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     120099910   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     120099910 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 CCP_MauG ComZ Motif Other DBs NCBI-GeneID:  120099910 NCBI-ProteinID:  XP_038957062 RGD:  41120816 LinkDB All DBs Position 1:complement(177095031..177095315) Genome browser AA seq 94 aa AA seqDB search MGDVVKGKKTSVQKCAQCHTVEKGGKHETGPKLHGLFGRKTGQAAGASYTDVNKNKGITW GEDTLMEYLEIPRKYIPETKMIFTGIKKKGKGQT NT seq 285 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgtaaaaggcaagaagacttctgttcagaagtgtgcccaatgccacact gtggaaaagggaggcaagcatgagactggaccaaagctccatggtctgtttgggcggaag acaggccaggctgctggggcctcttacacagatgtcaacaagaacaaaggcatcacctgg ggagaggataccctgatggagtatttggagattcccagaaagtacatccctgaaacaaaa atgatcttcactggaattaagaagaagggaaaagggcagacctaa

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