Myotis yumanensis (Yuma myotis): 139022150 Help Entry 139022150         CDS       T10762                                  Name (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism myum  Myotis yumanensis (Yuma myotis) Pathway myum00190   Oxidative phosphorylation myum01100   Metabolic pathways myum01524   Platinum drug resistance myum04115   p53 signaling pathway myum04210   Apoptosis myum04215   Apoptosis - multiple species myum04932   Non-alcoholic fatty liver disease myum05010   Alzheimer disease myum05012   Parkinson disease myum05014   Amyotrophic lateral sclerosis myum05016   Huntington disease myum05017   Spinocerebellar ataxia myum05020   Prion disease myum05022   Pathways of neurodegeneration - multiple diseases myum05132   Salmonella infection myum05134   Legionellosis myum05145   Toxoplasmosis myum05152   Tuberculosis myum05160   Hepatitis C myum05161   Hepatitis B myum05162   Measles myum05163   Human cytomegalovirus infection myum05164   Influenza A myum05167   Kaposi sarcoma-associated herpesvirus infection myum05168   Herpes simplex virus 1 infection myum05169   Epstein-Barr virus infection myum05170   Human immunodeficiency virus 1 infection myum05200   Pathways in cancer myum05210   Colorectal cancer myum05222   Small cell lung cancer myum05416   Viral myocarditis myum05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:myum00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     139022150  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     139022150    04215 Apoptosis - multiple species     139022150    04115 p53 signaling pathway     139022150  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     139022150   09162 Cancer: specific types    05210 Colorectal cancer     139022150    05222 Small cell lung cancer     139022150   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     139022150    05161 Hepatitis B     139022150    05160 Hepatitis C     139022150    05164 Influenza A     139022150    05162 Measles     139022150    05168 Herpes simplex virus 1 infection     139022150    05163 Human cytomegalovirus infection     139022150    05167 Kaposi sarcoma-associated herpesvirus infection     139022150    05169 Epstein-Barr virus infection     139022150   09171 Infectious disease: bacterial    05132 Salmonella infection     139022150    05134 Legionellosis     139022150    05152 Tuberculosis     139022150   09174 Infectious disease: parasitic    05145 Toxoplasmosis     139022150   09164 Neurodegenerative disease    05010 Alzheimer disease     139022150    05012 Parkinson disease     139022150    05014 Amyotrophic lateral sclerosis     139022150    05016 Huntington disease     139022150    05017 Spinocerebellar ataxia     139022150    05020 Prion disease     139022150    05022 Pathways of neurodegeneration - multiple diseases     139022150   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     139022150    05416 Viral myocarditis     139022150   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     139022150   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     139022150 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Motif Other DBs NCBI-GeneID:  139022150 NCBI-ProteinID:  XP_070289327 LinkDB All DBs Position Unknown AA seq 135 aa AA seqDB search MKQILKELESRTSGLRVGISVLRATNEPFKIGDVEEDKKILVQKCAQGHTVEKGGKHRTG PNLHGLFGRNTGQAPGFSYTDANKNKGITWGEATLMEHLENPKKYIPGTKMLFAGLEKSA ERTDLIAYLKKATHE NT seq 408 nt NT seq  +upstreamnt  +downstreamnt atgaagcaaatactaaaggagttagagagccggacatctggcttgcgagtgggaatctcc gtgttgcgcgcgactaacgagccatttaaaataggtgatgttgaggaggataagaagatt ttggttcagaagtgtgcccagggccatactgtggagaagggaggcaagcacaggactggg ccaaatctccatggtctctttgggcgaaacacaggtcaggcccctggattttcttacaca gatgccaacaagaacaaaggtatcacctggggagaggctacactgatggagcatttggag aatcccaagaagtacatccctggaacaaaaatgctcttcgctggccttgagaagagtgca gaaaggacagacttgatagcttatctcaaaaaagctactcatgagtaa

DBGET integrated database retrieval system