Sus scrofa (pig): 100170131
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Entry
100170131 CDS
T01009
Symbol
CYCS
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
ssc
Sus scrofa (pig)
Pathway
ssc00190
Oxidative phosphorylation
ssc01100
Metabolic pathways
ssc01524
Platinum drug resistance
ssc04115
p53 signaling pathway
ssc04210
Apoptosis
ssc04215
Apoptosis - multiple species
ssc04932
Non-alcoholic fatty liver disease
ssc05010
Alzheimer disease
ssc05012
Parkinson disease
ssc05014
Amyotrophic lateral sclerosis
ssc05016
Huntington disease
ssc05017
Spinocerebellar ataxia
ssc05020
Prion disease
ssc05022
Pathways of neurodegeneration - multiple diseases
ssc05132
Salmonella infection
ssc05134
Legionellosis
ssc05145
Toxoplasmosis
ssc05152
Tuberculosis
ssc05160
Hepatitis C
ssc05161
Hepatitis B
ssc05162
Measles
ssc05163
Human cytomegalovirus infection
ssc05164
Influenza A
ssc05167
Kaposi sarcoma-associated herpesvirus infection
ssc05168
Herpes simplex virus 1 infection
ssc05169
Epstein-Barr virus infection
ssc05170
Human immunodeficiency virus 1 infection
ssc05200
Pathways in cancer
ssc05210
Colorectal cancer
ssc05222
Small cell lung cancer
ssc05416
Viral myocarditis
ssc05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
ssc00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
100170131 (CYCS)
09140 Cellular Processes
09143 Cell growth and death
04215 Apoptosis - multiple species
100170131 (CYCS)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100170131 (CYCS)
09162 Cancer: specific types
05210 Colorectal cancer
100170131 (CYCS)
05222 Small cell lung cancer
100170131 (CYCS)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100170131 (CYCS)
05161 Hepatitis B
100170131 (CYCS)
05160 Hepatitis C
100170131 (CYCS)
05164 Influenza A
100170131 (CYCS)
05162 Measles
100170131 (CYCS)
05163 Human cytomegalovirus infection
100170131 (CYCS)
05167 Kaposi sarcoma-associated herpesvirus infection
100170131 (CYCS)
05169 Epstein-Barr virus infection
100170131 (CYCS)
09171 Infectious disease: bacterial
05134 Legionellosis
100170131 (CYCS)
05152 Tuberculosis
100170131 (CYCS)
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100170131 (CYCS)
09164 Neurodegenerative disease
05010 Alzheimer disease
100170131 (CYCS)
05012 Parkinson disease
100170131 (CYCS)
05014 Amyotrophic lateral sclerosis
100170131 (CYCS)
05016 Huntington disease
100170131 (CYCS)
05017 Spinocerebellar ataxia
100170131 (CYCS)
05020 Prion disease
100170131 (CYCS)
05022 Pathways of neurodegeneration - multiple diseases
100170131 (CYCS)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100170131 (CYCS)
05416 Viral myocarditis
100170131 (CYCS)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100170131 (CYCS)
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100170131 (CYCS)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
100170131
NCBI-ProteinID:
NP_001123442
Ensembl:
ENSSSCG00000016714
UniProt:
P62895
Structure
PDB
PDBj
LinkDB
All DBs
Position
18:47169921..47172212
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKKGEREDLIAYLKKATNE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccacact
gtagaaaagggaggcaaacacaagactggtccaaacctccatggtctctttgggcggaag
acaggtcaggctcctggattctcttacacagatgccaacaagaacaaaggcatcacctgg
ggagaggagacactgatggagtacctggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagaagggagaaagggaagacttgatagcttatctgaaa
aaagctactaatgagtaa
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