Mustela nigripes (black-footed ferret): 132015876 Help Entry 132015876         CDS       T09425                                  Name (RefSeq) cytochrome c   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     132015876  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     132015876    04215 Apoptosis - multiple species     132015876    04115 p53 signaling pathway     132015876  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     132015876   09162 Cancer: specific types    05210 Colorectal cancer     132015876    05222 Small cell lung cancer     132015876   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     132015876    05161 Hepatitis B     132015876    05160 Hepatitis C     132015876    05164 Influenza A     132015876    05162 Measles     132015876    05168 Herpes simplex virus 1 infection     132015876    05163 Human cytomegalovirus infection     132015876    05167 Kaposi sarcoma-associated herpesvirus infection     132015876    05169 Epstein-Barr virus infection     132015876   09171 Infectious disease: bacterial    05132 Salmonella infection     132015876    05134 Legionellosis     132015876    05152 Tuberculosis     132015876   09174 Infectious disease: parasitic    05145 Toxoplasmosis     132015876   09164 Neurodegenerative disease    05010 Alzheimer disease     132015876    05012 Parkinson disease     132015876    05014 Amyotrophic lateral sclerosis     132015876    05016 Huntington disease     132015876    05017 Spinocerebellar ataxia     132015876    05020 Prion disease     132015876    05022 Pathways of neurodegeneration - multiple diseases     132015876   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     132015876    05416 Viral myocarditis     132015876   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     132015876   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     132015876 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  132015876 NCBI-ProteinID:  XP_059252694 LinkDB All DBs Position 4:50326786..50329318 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

DBGET integrated database retrieval system