Macaca mulatta (rhesus monkey): 701246
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Entry
701246 CDS
T01028
Name
(RefSeq) cytochrome c-like
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
701246
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
701246
04215 Apoptosis - multiple species
701246
04115 p53 signaling pathway
701246
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
701246
09162 Cancer: specific types
05210 Colorectal cancer
701246
05222 Small cell lung cancer
701246
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
701246
05161 Hepatitis B
701246
05160 Hepatitis C
701246
05164 Influenza A
701246
05162 Measles
701246
05168 Herpes simplex virus 1 infection
701246
05163 Human cytomegalovirus infection
701246
05167 Kaposi sarcoma-associated herpesvirus infection
701246
05169 Epstein-Barr virus infection
701246
09171 Infectious disease: bacterial
05132 Salmonella infection
701246
05134 Legionellosis
701246
05152 Tuberculosis
701246
09174 Infectious disease: parasitic
05145 Toxoplasmosis
701246
09164 Neurodegenerative disease
05010 Alzheimer disease
701246
05012 Parkinson disease
701246
05014 Amyotrophic lateral sclerosis
701246
05016 Huntington disease
701246
05017 Spinocerebellar ataxia
701246
05020 Prion disease
701246
05022 Pathways of neurodegeneration - multiple diseases
701246
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
701246
05416 Viral myocarditis
701246
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
701246
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
701246
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
701246
NCBI-ProteinID:
XP_001089569
Ensembl:
ENSMMUG00000016443
LinkDB
All DBs
Position
14:complement(51166589..51167792)
Genome browser
AA seq
128 aa
AA seq
DB search
MREWGRPASEQESSLRQRLKRELNMGDVEKGKKIFIMKCSQCHTVEKGGKHKTEPNLHGL
FGRKTGQARGYSYTAASKNKGITWGEDTLMKYFENLKKYIPGTKMIFVGIKKEERADLIA
YLKKATNE
NT seq
387 nt
NT seq
+upstream
nt +downstream
nt
atgagagagtggggacgtcctgcttcggagcaggaatcttcgttgcgccagcgactaaaa
agagaattaaatatgggtgatgttgagaaaggcaagaagatttttattatgaagtgttcc
cagtgccacactgttgaaaagggaggcaagcacaagactgagccaaatctccatggtctc
tttgggaggaagacaggtcaggcccgtggatactcttacacagccgccagtaagaacaaa
ggcatcacctggggagaggatacactgatgaaatatttcgagaatctcaagaagtacatc
cctggaacaaaaatgatctttgtcggcattaagaaggaagaaagggcagacttgatagct
tatctcaaaaaagctactaatgagtaa
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integrated database retrieval system