Neogale vison (American mink): 122904917 Help Entry 122904917         CDS       T08764                                  Name (RefSeq) cytochrome c   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     122904917  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     122904917    04215 Apoptosis - multiple species     122904917    04115 p53 signaling pathway     122904917  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     122904917   09162 Cancer: specific types    05210 Colorectal cancer     122904917    05222 Small cell lung cancer     122904917   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     122904917    05161 Hepatitis B     122904917    05160 Hepatitis C     122904917    05164 Influenza A     122904917    05162 Measles     122904917    05168 Herpes simplex virus 1 infection     122904917    05163 Human cytomegalovirus infection     122904917    05167 Kaposi sarcoma-associated herpesvirus infection     122904917    05169 Epstein-Barr virus infection     122904917   09171 Infectious disease: bacterial    05132 Salmonella infection     122904917    05134 Legionellosis     122904917    05152 Tuberculosis     122904917   09174 Infectious disease: parasitic    05145 Toxoplasmosis     122904917   09164 Neurodegenerative disease    05010 Alzheimer disease     122904917    05012 Parkinson disease     122904917    05014 Amyotrophic lateral sclerosis     122904917    05016 Huntington disease     122904917    05017 Spinocerebellar ataxia     122904917    05020 Prion disease     122904917    05022 Pathways of neurodegeneration - multiple diseases     122904917   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     122904917    05416 Viral myocarditis     122904917   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     122904917   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     122904917 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  122904917 NCBI-ProteinID:  XP_044102183 LinkDB All DBs Position 4:complement(180881237..180883767) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatacc gtggaaaagggaggcaagcacaagactgggccaaatctccatggtttatttggccgaaag accggtcaggcccctggattttcttacacggatgccaacaagaataaaggcatcacctgg ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctgggacaaaa atgatcttcgctggcattaagaagacaggggaaagagcagacttgatagcttatctcaaa aaagctactaaggagtaa

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