Microcebus murinus (gray mouse lemur): 105875906 Help Entry 105875906         CDS       T07238                                  Name (RefSeq) cytochrome c, somatic   KO K08738   cytochrome c Organism mmur  Microcebus murinus (gray mouse lemur) Pathway mmur00190   Oxidative phosphorylation mmur01100   Metabolic pathways mmur01524   Platinum drug resistance mmur04115   p53 signaling pathway mmur04210   Apoptosis mmur04215   Apoptosis - multiple species mmur04932   Non-alcoholic fatty liver disease mmur05010   Alzheimer disease mmur05012   Parkinson disease mmur05014   Amyotrophic lateral sclerosis mmur05016   Huntington disease mmur05017   Spinocerebellar ataxia mmur05020   Prion disease mmur05022   Pathways of neurodegeneration - multiple diseases mmur05132   Salmonella infection mmur05134   Legionellosis mmur05145   Toxoplasmosis mmur05152   Tuberculosis mmur05160   Hepatitis C mmur05161   Hepatitis B mmur05162   Measles mmur05163   Human cytomegalovirus infection mmur05164   Influenza A mmur05167   Kaposi sarcoma-associated herpesvirus infection mmur05168   Herpes simplex virus 1 infection mmur05169   Epstein-Barr virus infection mmur05170   Human immunodeficiency virus 1 infection mmur05200   Pathways in cancer mmur05210   Colorectal cancer mmur05222   Small cell lung cancer mmur05416   Viral myocarditis mmur05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:mmur00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     105875906  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     105875906    04215 Apoptosis - multiple species     105875906    04115 p53 signaling pathway     105875906  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     105875906   09162 Cancer: specific types    05210 Colorectal cancer     105875906    05222 Small cell lung cancer     105875906   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     105875906    05161 Hepatitis B     105875906    05160 Hepatitis C     105875906    05164 Influenza A     105875906    05162 Measles     105875906    05168 Herpes simplex virus 1 infection     105875906    05163 Human cytomegalovirus infection     105875906    05167 Kaposi sarcoma-associated herpesvirus infection     105875906    05169 Epstein-Barr virus infection     105875906   09171 Infectious disease: bacterial    05132 Salmonella infection     105875906    05134 Legionellosis     105875906    05152 Tuberculosis     105875906   09174 Infectious disease: parasitic    05145 Toxoplasmosis     105875906   09164 Neurodegenerative disease    05010 Alzheimer disease     105875906    05012 Parkinson disease     105875906    05014 Amyotrophic lateral sclerosis     105875906    05016 Huntington disease     105875906    05017 Spinocerebellar ataxia     105875906    05020 Prion disease     105875906    05022 Pathways of neurodegeneration - multiple diseases     105875906   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     105875906    05416 Viral myocarditis     105875906   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     105875906   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     105875906 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  105875906 NCBI-ProteinID:  XP_012628786 Ensembl:  ENSMICG00000045862 UniProt:  A0A8B7GYN3 LinkDB All DBs Position 11:complement(79279434..79281940) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAAGFSYTDANKNKGITW GEDTLMEYLENPKKYIPGTKMIFAGIKKKGERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttgttcagaagtgtgcccagtgccacact gtggaaaagggaggcaagcacaagactgggccaaatctccatggtctctttgggagaaag acaggtcaggctgctggattctcttacacagacgccaataagaacaaaggcatcacctgg ggagaggacacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatcttcgccggcattaagaagaagggagaaagggcagacttgatagcttatctcaaa aaagccactaatgagtaa

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