Mustela lutreola (European mink): 131829521
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Entry
131829521 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
131829521
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
131829521
04215 Apoptosis - multiple species
131829521
04115 p53 signaling pathway
131829521
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
131829521
09162 Cancer: specific types
05210 Colorectal cancer
131829521
05222 Small cell lung cancer
131829521
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
131829521
05161 Hepatitis B
131829521
05160 Hepatitis C
131829521
05164 Influenza A
131829521
05162 Measles
131829521
05168 Herpes simplex virus 1 infection
131829521
05163 Human cytomegalovirus infection
131829521
05167 Kaposi sarcoma-associated herpesvirus infection
131829521
05169 Epstein-Barr virus infection
131829521
09171 Infectious disease: bacterial
05132 Salmonella infection
131829521
05134 Legionellosis
131829521
05152 Tuberculosis
131829521
09174 Infectious disease: parasitic
05145 Toxoplasmosis
131829521
09164 Neurodegenerative disease
05010 Alzheimer disease
131829521
05012 Parkinson disease
131829521
05014 Amyotrophic lateral sclerosis
131829521
05016 Huntington disease
131829521
05017 Spinocerebellar ataxia
131829521
05020 Prion disease
131829521
05022 Pathways of neurodegeneration - multiple diseases
131829521
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
131829521
05416 Viral myocarditis
131829521
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
131829521
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
131829521
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
131829521
NCBI-ProteinID:
XP_059027371
LinkDB
All DBs
Position
4:complement(151894694..151897279)
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKTGERADLIAYLKKATKE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatacc
gtggaaaagggaggcaagcacaagactgggccaaatctccatggtttatttggccgaaag
accggtcaggcccctggattttcttacacggatgccaacaagaataaaggcatcacctgg
ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctgggacaaaa
atgatcttcgctggcattaagaagacaggggaaagagcagacttgatagcttatctcaaa
aaagctactaaggagtaa
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