Mustela nigripes (black-footed ferret): 132013022 Help Entry 132013022         CDS       T09425                                  Name (RefSeq) cytochrome c, testis-specific   KO K08738   cytochrome c Organism mnp  Mustela nigripes (black-footed ferret) Pathway mnp00190   Oxidative phosphorylation mnp01100   Metabolic pathways mnp01524   Platinum drug resistance mnp04115   p53 signaling pathway mnp04210   Apoptosis mnp04215   Apoptosis - multiple species mnp04932   Non-alcoholic fatty liver disease mnp05010   Alzheimer disease mnp05012   Parkinson disease mnp05014   Amyotrophic lateral sclerosis mnp05016   Huntington disease mnp05017   Spinocerebellar ataxia mnp05020   Prion disease mnp05022   Pathways of neurodegeneration - multiple diseases mnp05132   Salmonella infection mnp05134   Legionellosis mnp05145   Toxoplasmosis mnp05152   Tuberculosis mnp05160   Hepatitis C mnp05161   Hepatitis B mnp05162   Measles mnp05163   Human cytomegalovirus infection mnp05164   Influenza A mnp05167   Kaposi sarcoma-associated herpesvirus infection mnp05168   Herpes simplex virus 1 infection mnp05169   Epstein-Barr virus infection mnp05170   Human immunodeficiency virus 1 infection mnp05200   Pathways in cancer mnp05210   Colorectal cancer mnp05222   Small cell lung cancer mnp05416   Viral myocarditis mnp05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:mnp00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     132013022  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     132013022    04215 Apoptosis - multiple species     132013022    04115 p53 signaling pathway     132013022  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     132013022   09162 Cancer: specific types    05210 Colorectal cancer     132013022    05222 Small cell lung cancer     132013022   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     132013022    05161 Hepatitis B     132013022    05160 Hepatitis C     132013022    05164 Influenza A     132013022    05162 Measles     132013022    05168 Herpes simplex virus 1 infection     132013022    05163 Human cytomegalovirus infection     132013022    05167 Kaposi sarcoma-associated herpesvirus infection     132013022    05169 Epstein-Barr virus infection     132013022   09171 Infectious disease: bacterial    05132 Salmonella infection     132013022    05134 Legionellosis     132013022    05152 Tuberculosis     132013022   09174 Infectious disease: parasitic    05145 Toxoplasmosis     132013022   09164 Neurodegenerative disease    05010 Alzheimer disease     132013022    05012 Parkinson disease     132013022    05014 Amyotrophic lateral sclerosis     132013022    05016 Huntington disease     132013022    05017 Spinocerebellar ataxia     132013022    05020 Prion disease     132013022    05022 Pathways of neurodegeneration - multiple diseases     132013022   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     132013022    05416 Viral myocarditis     132013022   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     132013022   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     132013022 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  132013022 NCBI-ProteinID:  XP_059248783 LinkDB All DBs Position 3:complement(72712212..72724686) Genome browser AA seq 105 aa AA seqDB search MGDAEAGKKIFIQKCAQCHTVEKGGKHKVGPNLWGLFGRKTGQAPGFSYSDANKNKGVIW GEETLMEYLENPKKYIPGTKMVFAGLKKKSEREDLIQYLKQATSS NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggagatgctgaagcaggcaagaagatctttattcaaaaatgtgctcagtgccacaca gtggaaaaaggtggaaaacacaaggttggtccaaatctctggggtctttttggacgaaaa acaggacaagcaccaggattttcttattcagatgctaacaaaaacaaaggtgttatctgg ggagaggaaactctgatggaatatttggagaacccaaagaaatatatccctggaactaaa atggtctttgctggtcttaaaaagaagagtgagagagaagatcttattcagtatttgaaa caggcaacatcttcatga

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