Rhinopithecus roxellana (golden snub-nosed monkey): 104661761 Help Entry 104661761         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     104661761    04215 Apoptosis - multiple species     104661761    04115 p53 signaling pathway     104661761  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104661761   09162 Cancer: specific types    05210 Colorectal cancer     104661761    05222 Small cell lung cancer     104661761   09164 Neurodegenerative disease    05010 Alzheimer disease     104661761    05012 Parkinson disease     104661761    05014 Amyotrophic lateral sclerosis     104661761    05016 Huntington disease     104661761    05017 Spinocerebellar ataxia     104661761    05020 Prion disease     104661761    05022 Pathways of neurodegeneration - multiple diseases     104661761   09166 Cardiovascular disease    05416 Viral myocarditis     104661761   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     104661761   09171 Infectious disease: bacterial    05132 Salmonella infection     104661761    05134 Legionellosis     104661761    05152 Tuberculosis     104661761   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     104661761    05161 Hepatitis B     104661761    05160 Hepatitis C     104661761    05164 Influenza A     104661761    05162 Measles     104661761    05168 Herpes simplex virus 1 infection     104661761    05163 Human cytomegalovirus infection     104661761    05167 Kaposi sarcoma-associated herpesvirus infection     104661761    05169 Epstein-Barr virus infection     104661761   09174 Infectious disease: parasitic    05145 Toxoplasmosis     104661761   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     104661761 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 UPF0128 Motif Other DBs NCBI-GeneID:  104661761 NCBI-ProteinID:  XP_010360822 UniProt:  A0A2K6NSK5 LinkDB All DBs Position 20 AA seq 102 aa AA seqDB search MGDVEKGKKIFVQKCAQCHAMEKGGKHKTGPNLFGRKTGQAVGFSHTDASKNKGITWGED TLMEYLKNPKKYIPGTKMIFAGIKKEAERADLIAYLKKATNE NT seq 309 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttgttcagaagtgtgcccagtgccatgcc atggaaaagggaggcaagcataagactgggcctaatctcttcgggcggaagacaggtcag gccgttggattctctcacacagatgccagtaagaacaaaggcatcacctggggagaggat acactgatggagtatttgaagaatcccaagaagtacatccctggaacaaaaatgatcttt gccggcattaagaaggaggcagaaagggcagacttgatagcttatctcaaaaaagctact aatgagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104672188 Help Entry 104672188         CDS       T03989                                  Definition (RefSeq) cytochrome c   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     104672188    04215 Apoptosis - multiple species     104672188    04115 p53 signaling pathway     104672188  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104672188   09162 Cancer: specific types    05210 Colorectal cancer     104672188    05222 Small cell lung cancer     104672188   09164 Neurodegenerative disease    05010 Alzheimer disease     104672188    05012 Parkinson disease     104672188    05014 Amyotrophic lateral sclerosis     104672188    05016 Huntington disease     104672188    05017 Spinocerebellar ataxia     104672188    05020 Prion disease     104672188    05022 Pathways of neurodegeneration - multiple diseases     104672188   09166 Cardiovascular disease    05416 Viral myocarditis     104672188   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     104672188   09171 Infectious disease: bacterial    05132 Salmonella infection     104672188    05134 Legionellosis     104672188    05152 Tuberculosis     104672188   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     104672188    05161 Hepatitis B     104672188    05160 Hepatitis C     104672188    05164 Influenza A     104672188    05162 Measles     104672188    05168 Herpes simplex virus 1 infection     104672188    05163 Human cytomegalovirus infection     104672188    05167 Kaposi sarcoma-associated herpesvirus infection     104672188    05169 Epstein-Barr virus infection     104672188   09174 Infectious disease: parasitic    05145 Toxoplasmosis     104672188   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     104672188 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  104672188 NCBI-ProteinID:  XP_010374228 UniProt:  A0A2K6N726 LinkDB All DBs Position 6 AA seq 105 aa AA seqDB search MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa aaagctactaatgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 104679886 Help Entry 104679886         CDS       T03989                                  Definition (RefSeq) cytochrome c   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     104679886    04215 Apoptosis - multiple species     104679886    04115 p53 signaling pathway     104679886  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104679886   09162 Cancer: specific types    05210 Colorectal cancer     104679886    05222 Small cell lung cancer     104679886   09164 Neurodegenerative disease    05010 Alzheimer disease     104679886    05012 Parkinson disease     104679886    05014 Amyotrophic lateral sclerosis     104679886    05016 Huntington disease     104679886    05017 Spinocerebellar ataxia     104679886    05020 Prion disease     104679886    05022 Pathways of neurodegeneration - multiple diseases     104679886   09166 Cardiovascular disease    05416 Viral myocarditis     104679886   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     104679886   09171 Infectious disease: bacterial    05132 Salmonella infection     104679886    05134 Legionellosis     104679886    05152 Tuberculosis     104679886   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     104679886    05161 Hepatitis B     104679886    05160 Hepatitis C     104679886    05164 Influenza A     104679886    05162 Measles     104679886    05168 Herpes simplex virus 1 infection     104679886    05163 Human cytomegalovirus infection     104679886    05167 Kaposi sarcoma-associated herpesvirus infection     104679886    05169 Epstein-Barr virus infection     104679886   09174 Infectious disease: parasitic    05145 Toxoplasmosis     104679886   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     104679886 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  104679886 NCBI-ProteinID:  XP_010383921 UniProt:  A0A2K6N726 LinkDB All DBs Position 9 AA seq 105 aa AA seqDB search MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtacatcccgggaacaaaa atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa aaagctactaatgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 104681924 Help Entry 104681924         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     104681924    04215 Apoptosis - multiple species     104681924    04115 p53 signaling pathway     104681924  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104681924   09162 Cancer: specific types    05210 Colorectal cancer     104681924    05222 Small cell lung cancer     104681924   09164 Neurodegenerative disease    05010 Alzheimer disease     104681924    05012 Parkinson disease     104681924    05014 Amyotrophic lateral sclerosis     104681924    05016 Huntington disease     104681924    05017 Spinocerebellar ataxia     104681924    05020 Prion disease     104681924    05022 Pathways of neurodegeneration - multiple diseases     104681924   09166 Cardiovascular disease    05416 Viral myocarditis     104681924   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     104681924   09171 Infectious disease: bacterial    05132 Salmonella infection     104681924    05134 Legionellosis     104681924    05152 Tuberculosis     104681924   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     104681924    05161 Hepatitis B     104681924    05160 Hepatitis C     104681924    05164 Influenza A     104681924    05162 Measles     104681924    05168 Herpes simplex virus 1 infection     104681924    05163 Human cytomegalovirus infection     104681924    05167 Kaposi sarcoma-associated herpesvirus infection     104681924    05169 Epstein-Barr virus infection     104681924   09174 Infectious disease: parasitic    05145 Toxoplasmosis     104681924   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     104681924 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  104681924 NCBI-ProteinID:  XP_010386658 UniProt:  A0A2K6NB35 LinkDB All DBs Position 4 AA seq 105 aa AA seqDB search MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATKE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacact gttgaaaagggaggcaagcacaagactgggcctaatctccatggtctcttcgggcggaag acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatctttgttggcattaagaaaaaggaagaaagggcagacttgatagcttatctcaaa aaagctactaaagagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 115893266 Help Entry 115893266         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     115893266    04215 Apoptosis - multiple species     115893266    04115 p53 signaling pathway     115893266  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     115893266   09162 Cancer: specific types    05210 Colorectal cancer     115893266    05222 Small cell lung cancer     115893266   09164 Neurodegenerative disease    05010 Alzheimer disease     115893266    05012 Parkinson disease     115893266    05014 Amyotrophic lateral sclerosis     115893266    05016 Huntington disease     115893266    05017 Spinocerebellar ataxia     115893266    05020 Prion disease     115893266    05022 Pathways of neurodegeneration - multiple diseases     115893266   09166 Cardiovascular disease    05416 Viral myocarditis     115893266   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     115893266   09171 Infectious disease: bacterial    05132 Salmonella infection     115893266    05134 Legionellosis     115893266    05152 Tuberculosis     115893266   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     115893266    05161 Hepatitis B     115893266    05160 Hepatitis C     115893266    05164 Influenza A     115893266    05162 Measles     115893266    05168 Herpes simplex virus 1 infection     115893266    05163 Human cytomegalovirus infection     115893266    05167 Kaposi sarcoma-associated herpesvirus infection     115893266    05169 Epstein-Barr virus infection     115893266   09174 Infectious disease: parasitic    05145 Toxoplasmosis     115893266   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     115893266 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 UPF0128 Motif Other DBs NCBI-GeneID:  115893266 NCBI-ProteinID:  XP_030772697 LinkDB All DBs Position 14 AA seq 105 aa AA seqDB search MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTVANKNKGITW GEDTLMEYLENPKKYIPGRKMVFAGIKKKEERADLIAYLKKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag acaggtcaggcccctggatactcttacacagtcgccaataagaacaaaggcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaagaaaa atggtctttgctggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa aaagctactaatgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 115893541 Help Entry 115893541         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     115893541    04215 Apoptosis - multiple species     115893541    04115 p53 signaling pathway     115893541  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     115893541   09162 Cancer: specific types    05210 Colorectal cancer     115893541    05222 Small cell lung cancer     115893541   09164 Neurodegenerative disease    05010 Alzheimer disease     115893541    05012 Parkinson disease     115893541    05014 Amyotrophic lateral sclerosis     115893541    05016 Huntington disease     115893541    05017 Spinocerebellar ataxia     115893541    05020 Prion disease     115893541    05022 Pathways of neurodegeneration - multiple diseases     115893541   09166 Cardiovascular disease    05416 Viral myocarditis     115893541   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     115893541   09171 Infectious disease: bacterial    05132 Salmonella infection     115893541    05134 Legionellosis     115893541    05152 Tuberculosis     115893541   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     115893541    05161 Hepatitis B     115893541    05160 Hepatitis C     115893541    05164 Influenza A     115893541    05162 Measles     115893541    05168 Herpes simplex virus 1 infection     115893541    05163 Human cytomegalovirus infection     115893541    05167 Kaposi sarcoma-associated herpesvirus infection     115893541    05169 Epstein-Barr virus infection     115893541   09174 Infectious disease: parasitic    05145 Toxoplasmosis     115893541   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     115893541 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Motif Other DBs NCBI-GeneID:  115893541 NCBI-ProteinID:  XP_030773590 LinkDB All DBs Position 15 AA seq 113 aa AA seqDB search MDIKILLIKNKFGSRKKIFVQKCAHGHTVEKGGQHKTGPNLHSLFGWKTGEAVGFSYTDT SKNKGITWGKDTLMHYLEAPKNNIPGTKIISAGIKKKAERADLITNLKNATNE NT seq 342 nt NT seq  +upstreamnt  +downstreamnt atggacataaaaattctacttattaagaacaagtttggctctcgcaagaagatttttgtt cagaagtgtgcccacggccacacggtggaaaagggaggccagcacaagactgggcctaat ctccatagtctcttcgggtggaagacaggagaagctgttggattctcttacacagacacc agtaagaacaaaggcatcacctggggaaaggatacactgatgcactatttggaggctccc aagaacaacatcccgggaacaaaaattatctctgccggcattaagaagaaggcagaaagg gcagacttgataactaatctcaaaaacgctactaatgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 115894533 Help Entry 115894533         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     115894533    04215 Apoptosis - multiple species     115894533    04115 p53 signaling pathway     115894533  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     115894533   09162 Cancer: specific types    05210 Colorectal cancer     115894533    05222 Small cell lung cancer     115894533   09164 Neurodegenerative disease    05010 Alzheimer disease     115894533    05012 Parkinson disease     115894533    05014 Amyotrophic lateral sclerosis     115894533    05016 Huntington disease     115894533    05017 Spinocerebellar ataxia     115894533    05020 Prion disease     115894533    05022 Pathways of neurodegeneration - multiple diseases     115894533   09166 Cardiovascular disease    05416 Viral myocarditis     115894533   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     115894533   09171 Infectious disease: bacterial    05132 Salmonella infection     115894533    05134 Legionellosis     115894533    05152 Tuberculosis     115894533   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     115894533    05161 Hepatitis B     115894533    05160 Hepatitis C     115894533    05164 Influenza A     115894533    05162 Measles     115894533    05168 Herpes simplex virus 1 infection     115894533    05163 Human cytomegalovirus infection     115894533    05167 Kaposi sarcoma-associated herpesvirus infection     115894533    05169 Epstein-Barr virus infection     115894533   09174 Infectious disease: parasitic    05145 Toxoplasmosis     115894533   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     115894533 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 DUF3365 Motif Other DBs NCBI-GeneID:  115894533 NCBI-ProteinID:  XP_030777790 LinkDB All DBs Position 18 AA seq 105 aa AA seqDB search MGDVEKGKKIFVQKCAQCHTMEKGGKQKTGPNLHGLFGWKTGQAIGFSYIDTGKNKGITW GNDTLREYLENPRKYVPGTKMIFAGIKMKAERADLLAYLKKATSE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttgttcagaagtgtgcccagtgccacacc atggaaaagggaggcaagcaaaagactgggcctaatctccatggtctcttcgggtggaag acaggtcaggccattggattctcttacatagacaccggtaagaacaaaggcatcacctgg ggaaatgatacactgagggagtatttggagaatcccaggaaatacgttcctggaacaaaa atgatctttgccggcattaagatgaaggcagaaagggcagacttgttagcttatctcaaa aaagctacaagtgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 115898126 Help Entry 115898126         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     115898126    04215 Apoptosis - multiple species     115898126    04115 p53 signaling pathway     115898126  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     115898126   09162 Cancer: specific types    05210 Colorectal cancer     115898126    05222 Small cell lung cancer     115898126   09164 Neurodegenerative disease    05010 Alzheimer disease     115898126    05012 Parkinson disease     115898126    05014 Amyotrophic lateral sclerosis     115898126    05016 Huntington disease     115898126    05017 Spinocerebellar ataxia     115898126    05020 Prion disease     115898126    05022 Pathways of neurodegeneration - multiple diseases     115898126   09166 Cardiovascular disease    05416 Viral myocarditis     115898126   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     115898126   09171 Infectious disease: bacterial    05132 Salmonella infection     115898126    05134 Legionellosis     115898126    05152 Tuberculosis     115898126   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     115898126    05161 Hepatitis B     115898126    05160 Hepatitis C     115898126    05164 Influenza A     115898126    05162 Measles     115898126    05168 Herpes simplex virus 1 infection     115898126    05163 Human cytomegalovirus infection     115898126    05167 Kaposi sarcoma-associated herpesvirus infection     115898126    05169 Epstein-Barr virus infection     115898126   09174 Infectious disease: parasitic    05145 Toxoplasmosis     115898126   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     115898126 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  115898126 NCBI-ProteinID:  XP_030787682 LinkDB All DBs Position 6 AA seq 105 aa AA seqDB search MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW GEDTLMEYLENPKKYIPGTKMIFVGIKKKEEREDLIAYLRKATNE NT seq 318 nt NT seq  +upstreamnt  +downstreamnt atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg ggagaggacacactgatggaatatttggagaatcccaagaagtacatccctggaacaaaa atgatctttgtcggcattaagaagaaggaagaaagggaagacttgatagcttatctcaga aaagctactaatgagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 115899152 Help Entry 115899152         CDS       T03989                                  Definition (RefSeq) cytochrome c-like   KO K08738   cytochrome c Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro01524   Platinum drug resistance rro04115   p53 signaling pathway rro04210   Apoptosis rro04215   Apoptosis - multiple species rro04932   Non-alcoholic fatty liver disease rro05010   Alzheimer disease rro05012   Parkinson disease rro05014   Amyotrophic lateral sclerosis rro05016   Huntington disease rro05017   Spinocerebellar ataxia rro05020   Prion disease rro05022   Pathways of neurodegeneration - multiple diseases rro05132   Salmonella infection rro05134   Legionellosis rro05145   Toxoplasmosis rro05152   Tuberculosis rro05160   Hepatitis C rro05161   Hepatitis B rro05162   Measles rro05163   Human cytomegalovirus infection rro05164   Influenza A rro05167   Kaposi sarcoma-associated herpesvirus infection rro05168   Herpes simplex virus 1 infection rro05169   Epstein-Barr virus infection rro05170   Human immunodeficiency virus 1 infection rro05200   Pathways in cancer rro05210   Colorectal cancer rro05222   Small cell lung cancer rro05416   Viral myocarditis Brite KEGG Orthology (KO) [BR:rro00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     115899152    04215 Apoptosis - multiple species     115899152    04115 p53 signaling pathway     115899152  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     115899152   09162 Cancer: specific types    05210 Colorectal cancer     115899152    05222 Small cell lung cancer     115899152   09164 Neurodegenerative disease    05010 Alzheimer disease     115899152    05012 Parkinson disease     115899152    05014 Amyotrophic lateral sclerosis     115899152    05016 Huntington disease     115899152    05017 Spinocerebellar ataxia     115899152    05020 Prion disease     115899152    05022 Pathways of neurodegeneration - multiple diseases     115899152   09166 Cardiovascular disease    05416 Viral myocarditis     115899152   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     115899152   09171 Infectious disease: bacterial    05132 Salmonella infection     115899152    05134 Legionellosis     115899152    05152 Tuberculosis     115899152   09172 Infectious disease: viral    05170 Human immunodeficiency virus 1 infection     115899152    05161 Hepatitis B     115899152    05160 Hepatitis C     115899152    05164 Influenza A     115899152    05162 Measles     115899152    05168 Herpes simplex virus 1 infection     115899152    05163 Human cytomegalovirus infection     115899152    05167 Kaposi sarcoma-associated herpesvirus infection     115899152    05169 Epstein-Barr virus infection     115899152   09174 Infectious disease: parasitic    05145 Toxoplasmosis     115899152   09176 Drug resistance: antineoplastic    01524 Platinum drug resistance     115899152 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Motif Other DBs NCBI-GeneID:  115899152 NCBI-ProteinID:  XP_030792066 LinkDB All DBs Position 8 AA seq 104 aa AA seqDB search MGNVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGQKPGQAIGFSYTDANKNKCITW GEDTLMEYLENPKKYIPGTKMIFAGIKKKVEKADLTAYLKKATN NT seq 315 nt NT seq  +upstreamnt  +downstreamnt atgggtaatgttgagaaaggcaagaagatttttgttcagaagtgtgcccagtgtcacacc gtggaaaagggaggcaagcacaagactgggcctaatctccatggtctcttcgggcagaag ccaggtcaggccattggattctcttacacagatgccaataagaacaaatgcatcacctgg ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa atgatctttgccggcattaaaaagaaggtagaaaaggccgacttgacagcttatctcaaa aaagctactaattag

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