Mustela lutreola (European mink): 131829521 Help Entry 131829521         CDS       T09578                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism mlk  Mustela lutreola (European mink) Pathway mlk00190   Oxidative phosphorylation mlk01100   Metabolic pathways mlk01524   Platinum drug resistance mlk04115   p53 signaling pathway mlk04210   Apoptosis mlk04215   Apoptosis - multiple species mlk04932   Non-alcoholic fatty liver disease mlk05010   Alzheimer disease mlk05012   Parkinson disease mlk05014   Amyotrophic lateral sclerosis mlk05016   Huntington disease mlk05017   Spinocerebellar ataxia mlk05020   Prion disease mlk05022   Pathways of neurodegeneration - multiple diseases mlk05132   Salmonella infection mlk05134   Legionellosis mlk05145   Toxoplasmosis mlk05152   Tuberculosis mlk05160   Hepatitis C mlk05161   Hepatitis B mlk05162   Measles mlk05163   Human cytomegalovirus infection mlk05164   Influenza A mlk05167   Kaposi sarcoma-associated herpesvirus infection mlk05168   Herpes simplex virus 1 infection mlk05169   Epstein-Barr virus infection mlk05170   Human immunodeficiency virus 1 infection mlk05200   Pathways in cancer mlk05210   Colorectal cancer mlk05222   Small cell lung cancer mlk05416   Viral myocarditis mlk05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:mlk00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     131829521  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     131829521    04215 Apoptosis - multiple species     131829521    04115 p53 signaling pathway     131829521  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     131829521   09162 Cancer: specific types    05210 Colorectal cancer     131829521    05222 Small cell lung cancer     131829521   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     131829521    05161 Hepatitis B     131829521    05160 Hepatitis C     131829521    05164 Influenza A     131829521    05162 Measles     131829521    05168 Herpes simplex virus 1 infection     131829521    05163 Human cytomegalovirus infection     131829521    05167 Kaposi sarcoma-associated herpesvirus infection     131829521    05169 Epstein-Barr virus infection     131829521   09171 Infectious disease: bacterial    05132 Salmonella infection     131829521    05134 Legionellosis     131829521    05152 Tuberculosis     131829521   09174 Infectious disease: parasitic    05145 Toxoplasmosis     131829521   09164 Neurodegenerative disease    05010 Alzheimer disease     131829521    05012 Parkinson disease     131829521    05014 Amyotrophic lateral sclerosis     131829521    05016 Huntington disease     131829521    05017 Spinocerebellar ataxia     131829521    05020 Prion disease     131829521    05022 Pathways of neurodegeneration - multiple diseases     131829521   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     131829521    05416 Viral myocarditis     131829521   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     131829521   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     131829521 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  131829521 NCBI-ProteinID:  XP_059027371 LinkDB All DBs Position 4:complement(151894694..151897279) 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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