Prionailurus viverrinus (fishing cat): 125169849 Help Entry 125169849         CDS       T09889                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism pviv  Prionailurus viverrinus (fishing cat) Pathway pviv00190   Oxidative phosphorylation pviv01100   Metabolic pathways pviv01524   Platinum drug resistance pviv04115   p53 signaling pathway pviv04210   Apoptosis pviv04215   Apoptosis - multiple species pviv04932   Non-alcoholic fatty liver disease pviv05010   Alzheimer disease pviv05012   Parkinson disease pviv05014   Amyotrophic lateral sclerosis pviv05016   Huntington disease pviv05017   Spinocerebellar ataxia pviv05020   Prion disease pviv05022   Pathways of neurodegeneration - multiple diseases pviv05132   Salmonella infection pviv05134   Legionellosis pviv05145   Toxoplasmosis pviv05152   Tuberculosis pviv05160   Hepatitis C pviv05161   Hepatitis B pviv05162   Measles pviv05163   Human cytomegalovirus infection pviv05164   Influenza A pviv05167   Kaposi sarcoma-associated herpesvirus infection pviv05168   Herpes simplex virus 1 infection pviv05169   Epstein-Barr virus infection pviv05170   Human immunodeficiency virus 1 infection pviv05200   Pathways in cancer pviv05210   Colorectal cancer pviv05222   Small cell lung cancer pviv05416   Viral myocarditis pviv05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:pviv00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     125169849  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     125169849    04215 Apoptosis - multiple species     125169849    04115 p53 signaling pathway     125169849  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     125169849   09162 Cancer: specific types    05210 Colorectal cancer     125169849    05222 Small cell lung cancer     125169849   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     125169849    05161 Hepatitis B     125169849    05160 Hepatitis C     125169849    05164 Influenza A     125169849    05162 Measles     125169849    05168 Herpes simplex virus 1 infection     125169849    05163 Human cytomegalovirus infection     125169849    05167 Kaposi sarcoma-associated herpesvirus infection     125169849    05169 Epstein-Barr virus infection     125169849   09171 Infectious disease: bacterial    05132 Salmonella infection     125169849    05134 Legionellosis     125169849    05152 Tuberculosis     125169849   09174 Infectious disease: parasitic    05145 Toxoplasmosis     125169849   09164 Neurodegenerative disease    05010 Alzheimer disease     125169849    05012 Parkinson disease     125169849    05014 Amyotrophic lateral sclerosis     125169849    05016 Huntington disease     125169849    05017 Spinocerebellar ataxia     125169849    05020 Prion disease     125169849    05022 Pathways of neurodegeneration - multiple diseases     125169849   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     125169849    05416 Viral myocarditis     125169849   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     125169849   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     125169849 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 NCKAP5 CCP_MauG Motif Other DBs NCBI-GeneID:  125169849 NCBI-ProteinID:  XP_047721597 LinkDB All DBs Position B4:complement(51573171..51573488) Genome browser AA seq 105 aa AA seqDB search MGDIEKGKKIFVQKCAQCHTVETEGKHNTGPNLHGLFGRKTSQAPGFSYMDANKNKGITW GEETLMEYLENPKKYIPGTKMIFTGIKKSGERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatattgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaacggaaggcaagcacaacactgggccaaatctccatggtttatttgggcgaaag acaagtcaagcccctggattttcttacatggatgccaacaagaacaaaggcatcacctgg ggagaagagacactgatggagtatttggaaaatcccaagaagtacatccctggaacaaaa atgatcttcactggcattaagaagtcaggggaaagagcagacttgatagcttatctcaaa aaagctactaaggagtaa

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