Oryctolagus cuniculus (rabbit): 108178730 Help Entry 108178730         CDS       T03373                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu00190   Oxidative phosphorylation ocu01100   Metabolic pathways ocu01524   Platinum drug resistance ocu04115   p53 signaling pathway ocu04210   Apoptosis ocu04215   Apoptosis - multiple species ocu04932   Non-alcoholic fatty liver disease ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05014   Amyotrophic lateral sclerosis ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05132   Salmonella infection ocu05134   Legionellosis ocu05145   Toxoplasmosis ocu05152   Tuberculosis ocu05160   Hepatitis C ocu05161   Hepatitis B ocu05162   Measles ocu05163   Human cytomegalovirus infection ocu05164   Influenza A ocu05167   Kaposi sarcoma-associated herpesvirus infection ocu05168   Herpes simplex virus 1 infection ocu05169   Epstein-Barr virus infection ocu05170   Human immunodeficiency virus 1 infection ocu05200   Pathways in cancer ocu05210   Colorectal cancer ocu05222   Small cell lung cancer ocu05416   Viral myocarditis ocu05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:ocu00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     108178730  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     108178730    04215 Apoptosis - multiple species     108178730    04115 p53 signaling pathway     108178730  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     108178730   09162 Cancer: specific types    05210 Colorectal cancer     108178730    05222 Small cell lung cancer     108178730   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     108178730    05161 Hepatitis B     108178730    05160 Hepatitis C     108178730    05164 Influenza A     108178730    05162 Measles     108178730    05168 Herpes simplex virus 1 infection     108178730    05163 Human cytomegalovirus infection     108178730    05167 Kaposi sarcoma-associated herpesvirus infection     108178730    05169 Epstein-Barr virus infection     108178730   09171 Infectious disease: bacterial    05132 Salmonella infection     108178730    05134 Legionellosis     108178730    05152 Tuberculosis     108178730   09174 Infectious disease: parasitic    05145 Toxoplasmosis     108178730   09164 Neurodegenerative disease    05010 Alzheimer disease     108178730    05012 Parkinson disease     108178730    05014 Amyotrophic lateral sclerosis     108178730    05016 Huntington disease     108178730    05017 Spinocerebellar ataxia     108178730    05020 Prion disease     108178730    05022 Pathways of neurodegeneration - multiple diseases     108178730   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     108178730    05416 Viral myocarditis     108178730   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     108178730   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     108178730 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  108178730 NCBI-ProteinID:  XP_017205261 Ensembl:  ENSOCUG00000021641 UniProt:  G1TVV5 LinkDB All DBs Position X:complement(57284626..57284949) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVRKCAQCHTVEKGGKQKTGPNLHGLFGRKTGQAIGFSYTDTYKNKGNTW GEDILMEYLEKPKKYIPGTKMTLAGIKKKNERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttgttcggaaatgtgcccagtgccacact gtggaaaagggaggcaagcaaaagactggaccaaatctccatggtctgtttgggcggaag acaggtcaggccattggattctcctacacagacacctacaagaacaaaggcaacacctgg ggagaggacattctgatggagtatttggagaagcccaagaaatacatccctggaaccaaa atgaccttagctggcattaagaagaagaatgaaagggcagacttgatagcttatctcaaa aaagctacgaatgagtaa

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