Sus scrofa (pig): 100519295
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Entry
100519295 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
100519295
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
100519295
04215 Apoptosis - multiple species
100519295
04115 p53 signaling pathway
100519295
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100519295
09162 Cancer: specific types
05210 Colorectal cancer
100519295
05222 Small cell lung cancer
100519295
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100519295
05161 Hepatitis B
100519295
05160 Hepatitis C
100519295
05164 Influenza A
100519295
05162 Measles
100519295
05168 Herpes simplex virus 1 infection
100519295
05163 Human cytomegalovirus infection
100519295
05167 Kaposi sarcoma-associated herpesvirus infection
100519295
05169 Epstein-Barr virus infection
100519295
09171 Infectious disease: bacterial
05132 Salmonella infection
100519295
05134 Legionellosis
100519295
05152 Tuberculosis
100519295
09174 Infectious disease: parasitic
05145 Toxoplasmosis
100519295
09164 Neurodegenerative disease
05010 Alzheimer disease
100519295
05012 Parkinson disease
100519295
05014 Amyotrophic lateral sclerosis
100519295
05016 Huntington disease
100519295
05017 Spinocerebellar ataxia
100519295
05020 Prion disease
100519295
05022 Pathways of neurodegeneration - multiple diseases
100519295
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100519295
05416 Viral myocarditis
100519295
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
100519295
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
100519295
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Tll0287-like
Cytochrom_C550
CxC4
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
100519295
NCBI-ProteinID:
XP_003123169
Ensembl:
ENSSSCG00000024275
UniProt:
A0A4X1VKU6
I3LNY8
LinkDB
All DBs
Position
2:complement(72500149..72500463)
Genome browser
AA seq
104 aa
AA seq
DB search
MGDVEKNKIFVQKCAQCHTVEKGGKQKTGPNLHGLFGWNTGQTVGFSSVDVNKNKGITWG
EETLREYLEDRKKYIPGTKMIFVSIKKKGEKGDLIAYLKKAASE
NT seq
315 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagaacaagatttttgttcagaagtgtgcccagtgccatactgtg
gaaaagggaggcaagcagaaaactgggccaaacctccatggtctgtttgggtggaacaca
ggtcagactgttggattctcttccgtagatgtcaacaagaacaaaggcatcacctgggga
gaggagacgctgagggagtacttggaggatcgcaagaagtacatccctggaacaaaaatg
atctttgtcagcattaagaagaagggagaaaagggagacttgatagcttatctcaaaaaa
gctgctagtgaatag
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integrated database retrieval system