Physeter macrocephalus (sperm whale): 102978471 Help Entry 102978471         CDS       T06011                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism pcad  Physeter macrocephalus (sperm whale) Pathway pcad00190   Oxidative phosphorylation pcad01100   Metabolic pathways pcad01524   Platinum drug resistance pcad04115   p53 signaling pathway pcad04210   Apoptosis pcad04215   Apoptosis - multiple species pcad04932   Non-alcoholic fatty liver disease pcad05010   Alzheimer disease pcad05012   Parkinson disease pcad05014   Amyotrophic lateral sclerosis pcad05016   Huntington disease pcad05017   Spinocerebellar ataxia pcad05020   Prion disease pcad05022   Pathways of neurodegeneration - multiple diseases pcad05132   Salmonella infection pcad05134   Legionellosis pcad05145   Toxoplasmosis pcad05152   Tuberculosis pcad05160   Hepatitis C pcad05161   Hepatitis B pcad05162   Measles pcad05163   Human cytomegalovirus infection pcad05164   Influenza A pcad05167   Kaposi sarcoma-associated herpesvirus infection pcad05168   Herpes simplex virus 1 infection pcad05169   Epstein-Barr virus infection pcad05170   Human immunodeficiency virus 1 infection pcad05200   Pathways in cancer pcad05210   Colorectal cancer pcad05222   Small cell lung cancer pcad05416   Viral myocarditis pcad05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:pcad00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     102978471  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     102978471    04215 Apoptosis - multiple species     102978471    04115 p53 signaling pathway     102978471  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102978471   09162 Cancer: specific types    05210 Colorectal cancer     102978471    05222 Small cell lung cancer     102978471   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     102978471    05161 Hepatitis B     102978471    05160 Hepatitis C     102978471    05164 Influenza A     102978471    05162 Measles     102978471    05168 Herpes simplex virus 1 infection     102978471    05163 Human cytomegalovirus infection     102978471    05167 Kaposi sarcoma-associated herpesvirus infection     102978471    05169 Epstein-Barr virus infection     102978471   09171 Infectious disease: bacterial    05132 Salmonella infection     102978471    05134 Legionellosis     102978471    05152 Tuberculosis     102978471   09174 Infectious disease: parasitic    05145 Toxoplasmosis     102978471   09164 Neurodegenerative disease    05010 Alzheimer disease     102978471    05012 Parkinson disease     102978471    05014 Amyotrophic lateral sclerosis     102978471    05016 Huntington disease     102978471    05017 Spinocerebellar ataxia     102978471    05020 Prion disease     102978471    05022 Pathways of neurodegeneration - multiple diseases     102978471   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     102978471    05416 Viral myocarditis     102978471   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     102978471   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     102978471 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 DDE_Tnp_1 Motif Other DBs NCBI-GeneID:  102978471 NCBI-ProteinID:  XP_023978589 UniProt:  A0A2Y9SS80 LinkDB All DBs Position 6:complement(89643966..89644310) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGQKTGQPVGFSYTDANKNKGITG GEETLMECLETPKKYIPGTKMIFAGIKKKGERADLIAYLRKATNA NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggaggcaagcacaagactgggccaaatctccatggtctgtttgggcaaaag acaggtcagcctgtcggattctcttacactgatgccaacaagaacaaaggcatcaccggg ggagaggagacgctgatggagtgtttggagactcccaagaagtacatccctggaacaaaa atgatcttcgctggcattaagaagaagggagaaagggcagacttgatagcttatctcaga aaagctactaatgcgtaa

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