Equus asinus (ass): 106826627 Help Entry 106826627         CDS       T04645                                  Name (RefSeq) cytochrome c, testis-specific   KO K08738   cytochrome c Organism eai  Equus asinus (ass) Pathway eai00190   Oxidative phosphorylation eai01100   Metabolic pathways eai01524   Platinum drug resistance eai04115   p53 signaling pathway eai04210   Apoptosis eai04215   Apoptosis - multiple species eai04932   Non-alcoholic fatty liver disease eai05010   Alzheimer disease eai05012   Parkinson disease eai05014   Amyotrophic lateral sclerosis eai05016   Huntington disease eai05017   Spinocerebellar ataxia eai05020   Prion disease eai05022   Pathways of neurodegeneration - multiple diseases eai05132   Salmonella infection eai05134   Legionellosis eai05145   Toxoplasmosis eai05152   Tuberculosis eai05160   Hepatitis C eai05161   Hepatitis B eai05162   Measles eai05163   Human cytomegalovirus infection eai05164   Influenza A eai05167   Kaposi sarcoma-associated herpesvirus infection eai05168   Herpes simplex virus 1 infection eai05169   Epstein-Barr virus infection eai05170   Human immunodeficiency virus 1 infection eai05200   Pathways in cancer eai05210   Colorectal cancer eai05222   Small cell lung cancer eai05416   Viral myocarditis eai05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:eai00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     106826627  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     106826627    04215 Apoptosis - multiple species     106826627    04115 p53 signaling pathway     106826627  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     106826627   09162 Cancer: specific types    05210 Colorectal cancer     106826627    05222 Small cell lung cancer     106826627   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     106826627    05161 Hepatitis B     106826627    05160 Hepatitis C     106826627    05164 Influenza A     106826627    05162 Measles     106826627    05168 Herpes simplex virus 1 infection     106826627    05163 Human cytomegalovirus infection     106826627    05167 Kaposi sarcoma-associated herpesvirus infection     106826627    05169 Epstein-Barr virus infection     106826627   09171 Infectious disease: bacterial    05132 Salmonella infection     106826627    05134 Legionellosis     106826627    05152 Tuberculosis     106826627   09174 Infectious disease: parasitic    05145 Toxoplasmosis     106826627   09164 Neurodegenerative disease    05010 Alzheimer disease     106826627    05012 Parkinson disease     106826627    05014 Amyotrophic lateral sclerosis     106826627    05016 Huntington disease     106826627    05017 Spinocerebellar ataxia     106826627    05020 Prion disease     106826627    05022 Pathways of neurodegeneration - multiple diseases     106826627   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     106826627    05416 Viral myocarditis     106826627   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     106826627   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     106826627 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  106826627 NCBI-ProteinID:  XP_014689566 UniProt:  A0A9L0K2P8 LinkDB All DBs Position 4:35624528..35640816 Genome browser AA seq 104 aa AA seqDB search MGDAEAGKIFIQKCAQCHTVEKGGKHKTGPNLWGLFGRKTGQAPGFSYSDANKNKGVIWG EETLLEYLENPKKYIPGTKMIFAGLKKKNEREDLIQYLKRATSS NT seq 315 nt NT seq  +upstreamnt  +downstreamnt atgggagatgctgaagcaggcaagatctttattcaaaaatgtgctcagtgccacacagtg gaaaaaggtggaaaacacaagacaggtccaaatctctggggcctttttggccgaaaaaca ggacaagcaccaggattttcttactctgatgcaaacaaaaacaaaggtgttatctgggga gaggaaactctgttggaatatttggagaacccaaagaaatatatccctggaactaaaatg atctttgctggtcttaaaaagaagaatgagagagaagatcttattcagtatttgaaacgg gcaacatcttcataa

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