Lutra lutra (Eurasian river otter): 125082666 Help Entry 125082666         CDS       T08100                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism llv  Lutra lutra (Eurasian river otter) Pathway llv00190   Oxidative phosphorylation llv01100   Metabolic pathways llv01524   Platinum drug resistance llv04115   p53 signaling pathway llv04210   Apoptosis llv04215   Apoptosis - multiple species llv04932   Non-alcoholic fatty liver disease llv05010   Alzheimer disease llv05012   Parkinson disease llv05014   Amyotrophic lateral sclerosis llv05016   Huntington disease llv05017   Spinocerebellar ataxia llv05020   Prion disease llv05022   Pathways of neurodegeneration - multiple diseases llv05132   Salmonella infection llv05134   Legionellosis llv05145   Toxoplasmosis llv05152   Tuberculosis llv05160   Hepatitis C llv05161   Hepatitis B llv05162   Measles llv05163   Human cytomegalovirus infection llv05164   Influenza A llv05167   Kaposi sarcoma-associated herpesvirus infection llv05168   Herpes simplex virus 1 infection llv05169   Epstein-Barr virus infection llv05170   Human immunodeficiency virus 1 infection llv05200   Pathways in cancer llv05210   Colorectal cancer llv05222   Small cell lung cancer llv05416   Viral myocarditis llv05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:llv00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     125082666  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     125082666    04215 Apoptosis - multiple species     125082666    04115 p53 signaling pathway     125082666  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     125082666   09162 Cancer: specific types    05210 Colorectal cancer     125082666    05222 Small cell lung cancer     125082666   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     125082666    05161 Hepatitis B     125082666    05160 Hepatitis C     125082666    05164 Influenza A     125082666    05162 Measles     125082666    05168 Herpes simplex virus 1 infection     125082666    05163 Human cytomegalovirus infection     125082666    05167 Kaposi sarcoma-associated herpesvirus infection     125082666    05169 Epstein-Barr virus infection     125082666   09171 Infectious disease: bacterial    05132 Salmonella infection     125082666    05134 Legionellosis     125082666    05152 Tuberculosis     125082666   09174 Infectious disease: parasitic    05145 Toxoplasmosis     125082666   09164 Neurodegenerative disease    05010 Alzheimer disease     125082666    05012 Parkinson disease     125082666    05014 Amyotrophic lateral sclerosis     125082666    05016 Huntington disease     125082666    05017 Spinocerebellar ataxia     125082666    05020 Prion disease     125082666    05022 Pathways of neurodegeneration - multiple diseases     125082666   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     125082666    05416 Viral myocarditis     125082666   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     125082666   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     125082666 SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Motif Other DBs NCBI-GeneID:  125082666 NCBI-ProteinID:  XP_047554484 LinkDB All DBs Position 12:49953760..49954263 Genome browser AA seq 103 aa AA seqDB search MGDIEKGKTLVQKYAQCHTMEKRGKHKTGPNLHGLFGQKAGQAPRFSYTDANNKGITWGE ETLMEYLENPKKYIPGAKMIFTGIKKTRKRADLIAYLKKATKE NT seq 312 nt NT seq  +upstreamnt  +downstreamnt atgggtgatattgagaagggcaagactttggttcagaaatatgcccagtgtcataccatg gaaaaaagaggcaagcacaaaactgggccaaatctccatggtttatttgggcaaaaggca ggtcaggcacctagattttcttacacagatgccaataacaaaggcatcacctggggagag gagacactgatggagtatttggagaatcccaagaagtacatccctggagcaaaaatgatc ttcactggcattaagaagacaaggaaaagagcagacttgatagcttatctcaaaaaagct actaaggagtaa

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