Otolemur garnettii (small-eared galago): 100961637
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Entry
100961637 CDS
T07855
Name
(RefSeq) cytochrome c, testis-specific
KO
K08738
cytochrome c
Organism
oga
Otolemur garnettii (small-eared galago)
Pathway
oga00190
Oxidative phosphorylation
oga01100
Metabolic pathways
oga01524
Platinum drug resistance
oga04115
p53 signaling pathway
oga04210
Apoptosis
oga04215
Apoptosis - multiple species
oga04932
Non-alcoholic fatty liver disease
oga05010
Alzheimer disease
oga05012
Parkinson disease
oga05014
Amyotrophic lateral sclerosis
oga05016
Huntington disease
oga05017
Spinocerebellar ataxia
oga05020
Prion disease
oga05022
Pathways of neurodegeneration - multiple diseases
oga05132
Salmonella infection
oga05134
Legionellosis
oga05145
Toxoplasmosis
oga05152
Tuberculosis
oga05160
Hepatitis C
oga05161
Hepatitis B
oga05162
Measles
oga05163
Human cytomegalovirus infection
oga05164
Influenza A
oga05167
Kaposi sarcoma-associated herpesvirus infection
oga05168
Herpes simplex virus 1 infection
oga05169
Epstein-Barr virus infection
oga05170
Human immunodeficiency virus 1 infection
oga05200
Pathways in cancer
oga05210
Colorectal cancer
oga05222
Small cell lung cancer
oga05416
Viral myocarditis
oga05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
oga00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
100961637
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
100961637
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100961637
09162 Cancer: specific types
05210 Colorectal cancer
100961637
05222 Small cell lung cancer
100961637
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100961637
05161 Hepatitis B
100961637
05160 Hepatitis C
100961637
05164 Influenza A
100961637
05162 Measles
100961637
05163 Human cytomegalovirus infection
100961637
05167 Kaposi sarcoma-associated herpesvirus infection
100961637
05169 Epstein-Barr virus infection
100961637
09171 Infectious disease: bacterial
05134 Legionellosis
100961637
05152 Tuberculosis
100961637
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100961637
09164 Neurodegenerative disease
05010 Alzheimer disease
100961637
05012 Parkinson disease
100961637
05014 Amyotrophic lateral sclerosis
100961637
05016 Huntington disease
100961637
05017 Spinocerebellar ataxia
100961637
05020 Prion disease
100961637
05022 Pathways of neurodegeneration - multiple diseases
100961637
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100961637
05416 Viral myocarditis
100961637
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100961637
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100961637
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
Motif
Other DBs
NCBI-GeneID:
100961637
NCBI-ProteinID:
XP_003791535
Ensembl:
ENSOGAG00000026648
UniProt:
H0XUY8
LinkDB
All DBs
Position
Unknown
AA seq
104 aa
AA seq
DB search
MGDAEAGKKIFVQKCAQCHTVEKGGKHKTGPNLWGLFGRQTGQSPGFSYSDANKNKGIIW
GEDTLMEYLENPKKYIPGTKMIFAGLKKKKEREDLIQYLKQATS
NT seq
315 nt
NT seq
+upstream
nt +downstream
nt
atgggagatgctgaagcaggcaagaagatcttcgttcaaaaatgtgctcagtgccacaca
gtggaaaaaggtggaaaacacaagactggtccaaatctctggggcctttttggccggcaa
acaggacagtcaccaggattttcttattctgatgcaaataaaaacaaaggtataatctgg
ggagaagacactctgatggaatatttggagaacccaaagaaatatatccctggaactaaa
atgatctttgctggtcttaaaaagaagaaagaaagagaagatcttattcaatatttgaaa
caggcaacttcttaa
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integrated database retrieval system