Capra hircus (goat): 102173997 Help Entry 102173997         CDS       T02910                                  Name (RefSeq) cytochrome c   KO K08738   cytochrome c Organism chx  Capra hircus (goat) Pathway chx00190   Oxidative phosphorylation chx01100   Metabolic pathways chx01524   Platinum drug resistance chx04115   p53 signaling pathway chx04210   Apoptosis chx04215   Apoptosis - multiple species chx04932   Non-alcoholic fatty liver disease chx05010   Alzheimer disease chx05012   Parkinson disease chx05014   Amyotrophic lateral sclerosis chx05016   Huntington disease chx05017   Spinocerebellar ataxia chx05020   Prion disease chx05022   Pathways of neurodegeneration - multiple diseases chx05132   Salmonella infection chx05134   Legionellosis chx05145   Toxoplasmosis chx05152   Tuberculosis chx05160   Hepatitis C chx05161   Hepatitis B chx05162   Measles chx05163   Human cytomegalovirus infection chx05164   Influenza A chx05167   Kaposi sarcoma-associated herpesvirus infection chx05168   Herpes simplex virus 1 infection chx05169   Epstein-Barr virus infection chx05170   Human immunodeficiency virus 1 infection chx05200   Pathways in cancer chx05210   Colorectal cancer chx05222   Small cell lung cancer chx05416   Viral myocarditis chx05417   Lipid and atherosclerosis Brite KEGG Orthology (KO) [BR:chx00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     102173997  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     102173997    04215 Apoptosis - multiple species     102173997    04115 p53 signaling pathway     102173997  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102173997   09162 Cancer: specific types    05210 Colorectal cancer     102173997    05222 Small cell lung cancer     102173997   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     102173997    05161 Hepatitis B     102173997    05160 Hepatitis C     102173997    05164 Influenza A     102173997    05162 Measles     102173997    05168 Herpes simplex virus 1 infection     102173997    05163 Human cytomegalovirus infection     102173997    05167 Kaposi sarcoma-associated herpesvirus infection     102173997    05169 Epstein-Barr virus infection     102173997   09171 Infectious disease: bacterial    05132 Salmonella infection     102173997    05134 Legionellosis     102173997    05152 Tuberculosis     102173997   09174 Infectious disease: parasitic    05145 Toxoplasmosis     102173997   09164 Neurodegenerative disease    05010 Alzheimer disease     102173997    05012 Parkinson disease     102173997    05014 Amyotrophic lateral sclerosis     102173997    05016 Huntington disease     102173997    05017 Spinocerebellar ataxia     102173997    05020 Prion disease     102173997    05022 Pathways of neurodegeneration - multiple diseases     102173997   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     102173997    05416 Viral myocarditis     102173997   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     102173997   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     102173997 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 CCP_MauG Motif Other DBs NCBI-GeneID:  102173997 NCBI-ProteinID:  XP_017902567 UniProt:  A0A0C4Y1X3 LinkDB All DBs Position 4:complement(49491848..49497463) Genome browser AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW GEETLMEYLENPKKYIPGTKMIFAGIKKKGEREDLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact gtggaaaagggagggaagcacaagactgggccaaacctccatggtctgtttggacgaaag acaggtcaggctcctggattctcttacacagatgccaacaaaaacaaaggtatcacctgg ggagaggagacgctgatggagtacttggagaatcccaagaagtacatccctggaaccaag atgatctttgctggcattaagaagaagggagagagggaggacttgatagcttatctcaaa aaagctaccaatgagtaa

DBGET integrated database retrieval system