Phocoena sinus (vaquita): 116752326 Help Entry 116752326         CDS       T07759                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism psiu  Phocoena sinus (vaquita) Pathway psiu00190   Oxidative phosphorylation psiu01100   Metabolic pathways psiu01524   Platinum drug resistance psiu04115   p53 signaling pathway psiu04210   Apoptosis psiu04215   Apoptosis - multiple species psiu04932   Non-alcoholic fatty liver disease psiu05010   Alzheimer disease psiu05012   Parkinson disease psiu05014   Amyotrophic lateral sclerosis psiu05016   Huntington disease psiu05017   Spinocerebellar ataxia psiu05020   Prion disease psiu05022   Pathways of neurodegeneration - multiple diseases psiu05132   Salmonella infection psiu05134   Legionellosis psiu05145   Toxoplasmosis psiu05152   Tuberculosis psiu05160   Hepatitis C psiu05161   Hepatitis B psiu05162   Measles psiu05163   Human cytomegalovirus infection psiu05164   Influenza A psiu05167   Kaposi sarcoma-associated herpesvirus infection psiu05168   Herpes simplex virus 1 infection psiu05169   Epstein-Barr virus infection psiu05170   Human immunodeficiency virus 1 infection psiu05200   Pathways in cancer psiu05210   Colorectal cancer psiu05222   Small cell lung cancer psiu05416   Viral myocarditis psiu05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:psiu00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     116752326  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     116752326    04215 Apoptosis - multiple species     116752326    04115 p53 signaling pathway     116752326  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     116752326   09162 Cancer: specific types    05210 Colorectal cancer     116752326    05222 Small cell lung cancer     116752326   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     116752326    05161 Hepatitis B     116752326    05160 Hepatitis C     116752326    05164 Influenza A     116752326    05162 Measles     116752326    05168 Herpes simplex virus 1 infection     116752326    05163 Human cytomegalovirus infection     116752326    05167 Kaposi sarcoma-associated herpesvirus infection     116752326    05169 Epstein-Barr virus infection     116752326   09171 Infectious disease: bacterial    05132 Salmonella infection     116752326    05134 Legionellosis     116752326    05152 Tuberculosis     116752326   09174 Infectious disease: parasitic    05145 Toxoplasmosis     116752326   09164 Neurodegenerative disease    05010 Alzheimer disease     116752326    05012 Parkinson disease     116752326    05014 Amyotrophic lateral sclerosis     116752326    05016 Huntington disease     116752326    05017 Spinocerebellar ataxia     116752326    05020 Prion disease     116752326    05022 Pathways of neurodegeneration - multiple diseases     116752326   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     116752326    05416 Viral myocarditis     116752326   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     116752326   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     116752326 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  116752326 NCBI-ProteinID:  XP_032485097 Ensembl:  ENSPSNG00000002419 LinkDB All DBs Position 3:92781724..92782672 Genome browser AA seq 105 aa AA seqDB search MSDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAVGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKKSERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgagtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaatctccatggtctgtttgggcgaaag acaggtcaggctgtcggattctcttacacagatgccaacaagaacaaaggcatcacctgg ggagaggagacgctgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaagaagtcagaaagggcagacttgatagcttatctcaaa aaagctactaatgagtaa

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