Ornithorhynchus anatinus (platypus): 100077443 Help Entry 100077443         CDS       T01045                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism oaa  Ornithorhynchus anatinus (platypus) Pathway oaa00190   Oxidative phosphorylation oaa01100   Metabolic pathways oaa01524   Platinum drug resistance oaa04115   p53 signaling pathway oaa04210   Apoptosis oaa04215   Apoptosis - multiple species oaa04932   Non-alcoholic fatty liver disease oaa05010   Alzheimer disease oaa05012   Parkinson disease oaa05014   Amyotrophic lateral sclerosis oaa05016   Huntington disease oaa05017   Spinocerebellar ataxia oaa05020   Prion disease oaa05022   Pathways of neurodegeneration - multiple diseases oaa05132   Salmonella infection oaa05134   Legionellosis oaa05145   Toxoplasmosis oaa05152   Tuberculosis oaa05160   Hepatitis C oaa05161   Hepatitis B oaa05162   Measles oaa05163   Human cytomegalovirus infection oaa05164   Influenza A oaa05167   Kaposi sarcoma-associated herpesvirus infection oaa05168   Herpes simplex virus 1 infection oaa05169   Epstein-Barr virus infection oaa05170   Human immunodeficiency virus 1 infection oaa05200   Pathways in cancer oaa05210   Colorectal cancer oaa05222   Small cell lung cancer oaa05416   Viral myocarditis oaa05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:oaa00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     100077443  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     100077443    04215 Apoptosis - multiple species     100077443    04115 p53 signaling pathway     100077443  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     100077443   09162 Cancer: specific types    05210 Colorectal cancer     100077443    05222 Small cell lung cancer     100077443   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     100077443    05161 Hepatitis B     100077443    05160 Hepatitis C     100077443    05164 Influenza A     100077443    05162 Measles     100077443    05168 Herpes simplex virus 1 infection     100077443    05163 Human cytomegalovirus infection     100077443    05167 Kaposi sarcoma-associated herpesvirus infection     100077443    05169 Epstein-Barr virus infection     100077443   09171 Infectious disease: bacterial    05132 Salmonella infection     100077443    05134 Legionellosis     100077443    05152 Tuberculosis     100077443   09174 Infectious disease: parasitic    05145 Toxoplasmosis     100077443   09164 Neurodegenerative disease    05010 Alzheimer disease     100077443    05012 Parkinson disease     100077443    05014 Amyotrophic lateral sclerosis     100077443    05016 Huntington disease     100077443    05017 Spinocerebellar ataxia     100077443    05020 Prion disease     100077443    05022 Pathways of neurodegeneration - multiple diseases     100077443   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     100077443    05416 Viral myocarditis     100077443   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     100077443   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     100077443 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  100077443 NCBI-ProteinID:  XP_028926987 LinkDB All DBs Position 8:57048857..57053122 Genome browser AA seq 105 aa AA seqDB search MGDFEKGKKIFVQKCAQCHTVEKGGKHKTGPNLNGLFGRKTGQAPGFSYTDANKSKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKKGERADLVAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgacttcgagaagggcaagaagatctttgtgcagaaatgcgcccagtgccacaca gtcgaaaagggaggcaagcacaagaccggacccaacctgaacggactgtttggacggaag actgggcaggctccaggttttagttatacagatgccaacaagagcaaaggcatcacctgg ggagaggaaacactgatggaatacttggaaaatcccaagaagtatatccctggcacaaaa atgatcttcgccggcattaagaagaagggcgaaagggcagacttggtagcatatctcaaa aaagccaccaaggagtaa

DBGET integrated database retrieval system