Macaca mulatta (rhesus monkey): 100425223
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Entry
100425223 CDS
T01028
Symbol
CYCS
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc00190
Oxidative phosphorylation
mcc01100
Metabolic pathways
mcc01524
Platinum drug resistance
mcc04115
p53 signaling pathway
mcc04210
Apoptosis
mcc04215
Apoptosis - multiple species
mcc04932
Non-alcoholic fatty liver disease
mcc05010
Alzheimer disease
mcc05012
Parkinson disease
mcc05014
Amyotrophic lateral sclerosis
mcc05016
Huntington disease
mcc05017
Spinocerebellar ataxia
mcc05020
Prion disease
mcc05022
Pathways of neurodegeneration - multiple diseases
mcc05132
Salmonella infection
mcc05134
Legionellosis
mcc05145
Toxoplasmosis
mcc05152
Tuberculosis
mcc05160
Hepatitis C
mcc05161
Hepatitis B
mcc05162
Measles
mcc05163
Human cytomegalovirus infection
mcc05164
Influenza A
mcc05167
Kaposi sarcoma-associated herpesvirus infection
mcc05168
Herpes simplex virus 1 infection
mcc05169
Epstein-Barr virus infection
mcc05170
Human immunodeficiency virus 1 infection
mcc05200
Pathways in cancer
mcc05210
Colorectal cancer
mcc05222
Small cell lung cancer
mcc05416
Viral myocarditis
mcc05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
100425223 (CYCS)
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
100425223 (CYCS)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100425223 (CYCS)
09162 Cancer: specific types
05210 Colorectal cancer
100425223 (CYCS)
05222 Small cell lung cancer
100425223 (CYCS)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100425223 (CYCS)
05161 Hepatitis B
100425223 (CYCS)
05160 Hepatitis C
100425223 (CYCS)
05164 Influenza A
100425223 (CYCS)
05162 Measles
100425223 (CYCS)
05163 Human cytomegalovirus infection
100425223 (CYCS)
05167 Kaposi sarcoma-associated herpesvirus infection
100425223 (CYCS)
05169 Epstein-Barr virus infection
100425223 (CYCS)
09171 Infectious disease: bacterial
05134 Legionellosis
100425223 (CYCS)
05152 Tuberculosis
100425223 (CYCS)
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100425223 (CYCS)
09164 Neurodegenerative disease
05010 Alzheimer disease
100425223 (CYCS)
05012 Parkinson disease
100425223 (CYCS)
05014 Amyotrophic lateral sclerosis
100425223 (CYCS)
05016 Huntington disease
100425223 (CYCS)
05017 Spinocerebellar ataxia
100425223 (CYCS)
05020 Prion disease
100425223 (CYCS)
05022 Pathways of neurodegeneration - multiple diseases
100425223 (CYCS)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100425223 (CYCS)
05416 Viral myocarditis
100425223 (CYCS)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100425223 (CYCS)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100425223 (CYCS)
BRITE hierarchy
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
100425223
NCBI-ProteinID:
XP_028701781
LinkDB
All DBs
Position
3:90025188..90027719
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFIMKCSQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGYSYTAANKNKGITW
GEDTLMEYLENPKKYIPGTKMIFVGIKKKEERADLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcccagtgccacacc
gttgaaaagggaggcaagcacaagactgggccaaatctccatggtctcttcgggcggaag
acaggtcaggcccctggatactcttacacagccgccaataagaacaaaggcatcacctgg
ggagaggatacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatctttgtcggcattaagaagaaggaagaaagggcagacttgatagcttatctcaaa
aaagctactaatgagtaa
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