Nomascus leucogenys (northern white-cheeked gibbon): 100580069
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Entry
100580069 CDS
T03265
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
nle
Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle00190
Oxidative phosphorylation
nle01100
Metabolic pathways
nle01524
Platinum drug resistance
nle04115
p53 signaling pathway
nle04210
Apoptosis
nle04215
Apoptosis - multiple species
nle04932
Non-alcoholic fatty liver disease
nle05010
Alzheimer disease
nle05012
Parkinson disease
nle05014
Amyotrophic lateral sclerosis
nle05016
Huntington disease
nle05017
Spinocerebellar ataxia
nle05020
Prion disease
nle05022
Pathways of neurodegeneration - multiple diseases
nle05132
Salmonella infection
nle05134
Legionellosis
nle05145
Toxoplasmosis
nle05152
Tuberculosis
nle05160
Hepatitis C
nle05161
Hepatitis B
nle05162
Measles
nle05163
Human cytomegalovirus infection
nle05164
Influenza A
nle05167
Kaposi sarcoma-associated herpesvirus infection
nle05168
Herpes simplex virus 1 infection
nle05169
Epstein-Barr virus infection
nle05170
Human immunodeficiency virus 1 infection
nle05200
Pathways in cancer
nle05210
Colorectal cancer
nle05222
Small cell lung cancer
nle05416
Viral myocarditis
nle05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
nle00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
100580069
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
100580069
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100580069
09162 Cancer: specific types
05210 Colorectal cancer
100580069
05222 Small cell lung cancer
100580069
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100580069
05161 Hepatitis B
100580069
05160 Hepatitis C
100580069
05164 Influenza A
100580069
05162 Measles
100580069
05163 Human cytomegalovirus infection
100580069
05167 Kaposi sarcoma-associated herpesvirus infection
100580069
05169 Epstein-Barr virus infection
100580069
09171 Infectious disease: bacterial
05134 Legionellosis
100580069
05152 Tuberculosis
100580069
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100580069
09164 Neurodegenerative disease
05010 Alzheimer disease
100580069
05012 Parkinson disease
100580069
05014 Amyotrophic lateral sclerosis
100580069
05016 Huntington disease
100580069
05017 Spinocerebellar ataxia
100580069
05020 Prion disease
100580069
05022 Pathways of neurodegeneration - multiple diseases
100580069
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100580069
05416 Viral myocarditis
100580069
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100580069
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100580069
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
100580069
NCBI-ProteinID:
XP_003270471
Ensembl:
ENSNLEG00000014901
UniProt:
G1RY04
LinkDB
All DBs
Position
17:80054930..80057378
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGIIW
GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc
gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag
acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcatctgg
ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa
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