Mustela lutreola (European mink): 131834139
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Entry
131834139 CDS
T09578
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
mlk
Mustela lutreola (European mink)
Pathway
mlk00190
Oxidative phosphorylation
mlk01100
Metabolic pathways
mlk01524
Platinum drug resistance
mlk04115
p53 signaling pathway
mlk04210
Apoptosis
mlk04215
Apoptosis - multiple species
mlk04932
Non-alcoholic fatty liver disease
mlk05010
Alzheimer disease
mlk05012
Parkinson disease
mlk05014
Amyotrophic lateral sclerosis
mlk05016
Huntington disease
mlk05017
Spinocerebellar ataxia
mlk05020
Prion disease
mlk05022
Pathways of neurodegeneration - multiple diseases
mlk05132
Salmonella infection
mlk05134
Legionellosis
mlk05145
Toxoplasmosis
mlk05152
Tuberculosis
mlk05160
Hepatitis C
mlk05161
Hepatitis B
mlk05162
Measles
mlk05163
Human cytomegalovirus infection
mlk05164
Influenza A
mlk05167
Kaposi sarcoma-associated herpesvirus infection
mlk05168
Herpes simplex virus 1 infection
mlk05169
Epstein-Barr virus infection
mlk05170
Human immunodeficiency virus 1 infection
mlk05200
Pathways in cancer
mlk05210
Colorectal cancer
mlk05222
Small cell lung cancer
mlk05416
Viral myocarditis
mlk05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
mlk00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
131834139
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
131834139
04215 Apoptosis - multiple species
131834139
04115 p53 signaling pathway
131834139
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
131834139
09162 Cancer: specific types
05210 Colorectal cancer
131834139
05222 Small cell lung cancer
131834139
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
131834139
05161 Hepatitis B
131834139
05160 Hepatitis C
131834139
05164 Influenza A
131834139
05162 Measles
131834139
05168 Herpes simplex virus 1 infection
131834139
05163 Human cytomegalovirus infection
131834139
05167 Kaposi sarcoma-associated herpesvirus infection
131834139
05169 Epstein-Barr virus infection
131834139
09171 Infectious disease: bacterial
05132 Salmonella infection
131834139
05134 Legionellosis
131834139
05152 Tuberculosis
131834139
09174 Infectious disease: parasitic
05145 Toxoplasmosis
131834139
09164 Neurodegenerative disease
05010 Alzheimer disease
131834139
05012 Parkinson disease
131834139
05014 Amyotrophic lateral sclerosis
131834139
05016 Huntington disease
131834139
05017 Spinocerebellar ataxia
131834139
05020 Prion disease
131834139
05022 Pathways of neurodegeneration - multiple diseases
131834139
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
131834139
05416 Viral myocarditis
131834139
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
131834139
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
131834139
BRITE hierarchy
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
131834139
NCBI-ProteinID:
XP_059034324
LinkDB
All DBs
Position
6:104316922..104317914
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKKATKE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatacc
gtggaaaagggaggcaagcacaagactgggccaaatctccatggtttatttggccgaaag
accggtcaggcccctggattttcttacacggatgccaacaaaaataaaggcatcacctgg
ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctgggacaaaa
atgatctttgctggcattaagaagacaggggaaagagcagacttgatagcttatctcaaa
aaagctactaaggagtaa
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