Sus scrofa (pig): 100621347
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Entry
100621347 CDS
T01009
Name
(RefSeq) cytochrome c-like
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
100621347
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
100621347
04215 Apoptosis - multiple species
100621347
04115 p53 signaling pathway
100621347
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100621347
09162 Cancer: specific types
05210 Colorectal cancer
100621347
05222 Small cell lung cancer
100621347
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100621347
05161 Hepatitis B
100621347
05160 Hepatitis C
100621347
05164 Influenza A
100621347
05162 Measles
100621347
05168 Herpes simplex virus 1 infection
100621347
05163 Human cytomegalovirus infection
100621347
05167 Kaposi sarcoma-associated herpesvirus infection
100621347
05169 Epstein-Barr virus infection
100621347
09171 Infectious disease: bacterial
05132 Salmonella infection
100621347
05134 Legionellosis
100621347
05152 Tuberculosis
100621347
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100621347
09164 Neurodegenerative disease
05010 Alzheimer disease
100621347
05012 Parkinson disease
100621347
05014 Amyotrophic lateral sclerosis
100621347
05016 Huntington disease
100621347
05017 Spinocerebellar ataxia
100621347
05020 Prion disease
100621347
05022 Pathways of neurodegeneration - multiple diseases
100621347
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100621347
05416 Viral myocarditis
100621347
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100621347
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100621347
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrom_C550
Cytochrome_CBB3
NCKAP5
Motif
Other DBs
NCBI-GeneID:
100621347
NCBI-ProteinID:
XP_013851692
UniProt:
A0A8W4FGU7
A0A4X1TFW9
LinkDB
All DBs
Position
3:109213776..109214078
Genome browser
AA seq
85 aa
AA seq
DB search
MGDVEQGKKIFVQKSAQCHAVEKGGKHKTGPNLHGLFGQKRGQAPGFSYPDANKNKGITW
GEETLMEYLENSKYIPGMKMIFAGI
NT seq
258 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagcagggcaagaagatttttgttcagaagagtgcccagtgccacgct
gtagaaaagggaggcaagcacaagactggtccaaacctccatggtctctttgggcagaag
agaggtcaggctcctggattctcttacccagatgccaacaagaacaaaggcatcacctgg
ggagaggagacactgatggagtacctggagaattccaagtacatccctggaatgaaaatg
atctttgctggcatttag
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integrated database retrieval system