Neogale vison (American mink): 122902631 Help Entry 122902631         CDS       T08764                                  Name (RefSeq) cytochrome c, testis-specific   KO K08738   cytochrome c Organism nvs  Neogale vison (American mink) Pathway nvs00190   Oxidative phosphorylation nvs01100   Metabolic pathways nvs01524   Platinum drug resistance nvs04115   p53 signaling pathway nvs04210   Apoptosis nvs04215   Apoptosis - multiple species nvs04932   Non-alcoholic fatty liver disease nvs05010   Alzheimer disease nvs05012   Parkinson disease nvs05014   Amyotrophic lateral sclerosis nvs05016   Huntington disease nvs05017   Spinocerebellar ataxia nvs05020   Prion disease nvs05022   Pathways of neurodegeneration - multiple diseases nvs05132   Salmonella infection nvs05134   Legionellosis nvs05145   Toxoplasmosis nvs05152   Tuberculosis nvs05160   Hepatitis C nvs05161   Hepatitis B nvs05162   Measles nvs05163   Human cytomegalovirus infection nvs05164   Influenza A nvs05167   Kaposi sarcoma-associated herpesvirus infection nvs05168   Herpes simplex virus 1 infection nvs05169   Epstein-Barr virus infection nvs05170   Human immunodeficiency virus 1 infection nvs05200   Pathways in cancer nvs05210   Colorectal cancer nvs05222   Small cell lung cancer nvs05416   Viral myocarditis nvs05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:nvs00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     122902631  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     122902631    04215 Apoptosis - multiple species     122902631    04115 p53 signaling pathway     122902631  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     122902631   09162 Cancer: specific types    05210 Colorectal cancer     122902631    05222 Small cell lung cancer     122902631   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     122902631    05161 Hepatitis B     122902631    05160 Hepatitis C     122902631    05164 Influenza A     122902631    05162 Measles     122902631    05168 Herpes simplex virus 1 infection     122902631    05163 Human cytomegalovirus infection     122902631    05167 Kaposi sarcoma-associated herpesvirus infection     122902631    05169 Epstein-Barr virus infection     122902631   09171 Infectious disease: bacterial    05132 Salmonella infection     122902631    05134 Legionellosis     122902631    05152 Tuberculosis     122902631   09174 Infectious disease: parasitic    05145 Toxoplasmosis     122902631   09164 Neurodegenerative disease    05010 Alzheimer disease     122902631    05012 Parkinson disease     122902631    05014 Amyotrophic lateral sclerosis     122902631    05016 Huntington disease     122902631    05017 Spinocerebellar ataxia     122902631    05020 Prion disease     122902631    05022 Pathways of neurodegeneration - multiple diseases     122902631   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     122902631    05416 Viral myocarditis     122902631   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     122902631   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     122902631 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  122902631 NCBI-ProteinID:  XP_044098341 UniProt:  A0A8C7AH20 LinkDB All DBs Position 3:complement(73991529..74007784) Genome browser AA seq 105 aa AA seqDB search MGDAEAGKKIFIQKCAQCHTVEKGGKHKVGPNLWGLFGRKTGQAPGFSYSDANKNKGVIW GEETLMEYLENPKKYIPGTKMVFAGLKKKSEREDLIQYLKQATSS NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggagatgctgaagcaggcaagaagatctttattcaaaaatgtgctcagtgccacaca gtggaaaaaggtggaaaacacaaggttggtccaaatctctggggtctttttggacgaaaa acaggacaagcaccaggattttcttattcagatgctaacaaaaacaaaggtgttatctgg ggagaggaaactctgatggaatatttggagaacccaaagaaatatatccctggaactaaa atggtctttgctggtcttaaaaagaagagtgagagagaagatcttattcaatatttgaaa caggcaacatcttcatga

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