Theropithecus gelada (gelada): 112605628
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Entry
112605628 CDS
T08041
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
tge
Theropithecus gelada (gelada)
Pathway
tge00190
Oxidative phosphorylation
tge01100
Metabolic pathways
tge01524
Platinum drug resistance
tge04115
p53 signaling pathway
tge04210
Apoptosis
tge04215
Apoptosis - multiple species
tge04932
Non-alcoholic fatty liver disease
tge05010
Alzheimer disease
tge05012
Parkinson disease
tge05014
Amyotrophic lateral sclerosis
tge05016
Huntington disease
tge05017
Spinocerebellar ataxia
tge05020
Prion disease
tge05022
Pathways of neurodegeneration - multiple diseases
tge05132
Salmonella infection
tge05134
Legionellosis
tge05145
Toxoplasmosis
tge05152
Tuberculosis
tge05160
Hepatitis C
tge05161
Hepatitis B
tge05162
Measles
tge05163
Human cytomegalovirus infection
tge05164
Influenza A
tge05167
Kaposi sarcoma-associated herpesvirus infection
tge05168
Herpes simplex virus 1 infection
tge05169
Epstein-Barr virus infection
tge05170
Human immunodeficiency virus 1 infection
tge05200
Pathways in cancer
tge05210
Colorectal cancer
tge05222
Small cell lung cancer
tge05416
Viral myocarditis
tge05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
tge00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
112605628
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
112605628
04215 Apoptosis - multiple species
112605628
04115 p53 signaling pathway
112605628
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112605628
09162 Cancer: specific types
05210 Colorectal cancer
112605628
05222 Small cell lung cancer
112605628
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
112605628
05161 Hepatitis B
112605628
05160 Hepatitis C
112605628
05164 Influenza A
112605628
05162 Measles
112605628
05168 Herpes simplex virus 1 infection
112605628
05163 Human cytomegalovirus infection
112605628
05167 Kaposi sarcoma-associated herpesvirus infection
112605628
05169 Epstein-Barr virus infection
112605628
09171 Infectious disease: bacterial
05132 Salmonella infection
112605628
05134 Legionellosis
112605628
05152 Tuberculosis
112605628
09174 Infectious disease: parasitic
05145 Toxoplasmosis
112605628
09164 Neurodegenerative disease
05010 Alzheimer disease
112605628
05012 Parkinson disease
112605628
05014 Amyotrophic lateral sclerosis
112605628
05016 Huntington disease
112605628
05017 Spinocerebellar ataxia
112605628
05020 Prion disease
112605628
05022 Pathways of neurodegeneration - multiple diseases
112605628
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
112605628
05416 Viral myocarditis
112605628
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
112605628
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
112605628
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
112605628
NCBI-ProteinID:
XP_025211072
Ensembl:
ENSTGEG00000013896
LinkDB
All DBs
Position
14:complement(51017905..51019154)
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQARGYSYTAASKNKGITW
GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacact
gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctctttgggaggaag
acaggtcaggcccgtggatactcttacacagccgccagtaagaacaaaggcatcacctgg
ggagaggatacactgatggaatatttggagaatcccaagaagtacatccctggaacaaaa
atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa
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integrated database retrieval system