Rhinolophus ferrumequinum (greater horseshoe bat): 117026373
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Entry
117026373 CDS
T07722
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
rfq
Rhinolophus ferrumequinum (greater horseshoe bat)
Pathway
rfq00190
Oxidative phosphorylation
rfq01100
Metabolic pathways
rfq01524
Platinum drug resistance
rfq04115
p53 signaling pathway
rfq04210
Apoptosis
rfq04215
Apoptosis - multiple species
rfq04932
Non-alcoholic fatty liver disease
rfq05010
Alzheimer disease
rfq05012
Parkinson disease
rfq05014
Amyotrophic lateral sclerosis
rfq05016
Huntington disease
rfq05017
Spinocerebellar ataxia
rfq05020
Prion disease
rfq05022
Pathways of neurodegeneration - multiple diseases
rfq05132
Salmonella infection
rfq05134
Legionellosis
rfq05145
Toxoplasmosis
rfq05152
Tuberculosis
rfq05160
Hepatitis C
rfq05161
Hepatitis B
rfq05162
Measles
rfq05163
Human cytomegalovirus infection
rfq05164
Influenza A
rfq05167
Kaposi sarcoma-associated herpesvirus infection
rfq05168
Herpes simplex virus 1 infection
rfq05169
Epstein-Barr virus infection
rfq05170
Human immunodeficiency virus 1 infection
rfq05200
Pathways in cancer
rfq05210
Colorectal cancer
rfq05222
Small cell lung cancer
rfq05416
Viral myocarditis
rfq05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
rfq00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
117026373
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
117026373
04215 Apoptosis - multiple species
117026373
04115 p53 signaling pathway
117026373
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117026373
09162 Cancer: specific types
05210 Colorectal cancer
117026373
05222 Small cell lung cancer
117026373
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
117026373
05161 Hepatitis B
117026373
05160 Hepatitis C
117026373
05164 Influenza A
117026373
05162 Measles
117026373
05168 Herpes simplex virus 1 infection
117026373
05163 Human cytomegalovirus infection
117026373
05167 Kaposi sarcoma-associated herpesvirus infection
117026373
05169 Epstein-Barr virus infection
117026373
09171 Infectious disease: bacterial
05132 Salmonella infection
117026373
05134 Legionellosis
117026373
05152 Tuberculosis
117026373
09174 Infectious disease: parasitic
05145 Toxoplasmosis
117026373
09164 Neurodegenerative disease
05010 Alzheimer disease
117026373
05012 Parkinson disease
117026373
05014 Amyotrophic lateral sclerosis
117026373
05016 Huntington disease
117026373
05017 Spinocerebellar ataxia
117026373
05020 Prion disease
117026373
05022 Pathways of neurodegeneration - multiple diseases
117026373
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
117026373
05416 Viral myocarditis
117026373
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
117026373
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
117026373
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
117026373
NCBI-ProteinID:
XP_032969023
Ensembl:
ENSRFEG00010004537
LinkDB
All DBs
Position
X:complement(54856808..54857218)
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKAGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKTAERADLIAYLKKATKE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgtgcagaagtgtgcccagtgccatact
gtggaaaaggcaggcaagcacaagactgggccaaatctccatggtctgtttgggcgaaag
actggtcaggcccctggattttcttacacggatgccaacaagaacaaaggtatcacctgg
ggagaagaaaccttgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaagactgcagaaagggcagacttgatagcgtatctcaaa
aaggctactaaggaataa
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