Panthera uncia (snow leopard): 125929995
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Entry
125929995 CDS
T08832
Name
(RefSeq) cytochrome c
KO
K08738
cytochrome c
Organism
puc
Panthera uncia (snow leopard)
Pathway
puc00190
Oxidative phosphorylation
puc01100
Metabolic pathways
puc01524
Platinum drug resistance
puc04115
p53 signaling pathway
puc04210
Apoptosis
puc04215
Apoptosis - multiple species
puc04932
Non-alcoholic fatty liver disease
puc05010
Alzheimer disease
puc05012
Parkinson disease
puc05014
Amyotrophic lateral sclerosis
puc05016
Huntington disease
puc05017
Spinocerebellar ataxia
puc05020
Prion disease
puc05022
Pathways of neurodegeneration - multiple diseases
puc05132
Salmonella infection
puc05134
Legionellosis
puc05145
Toxoplasmosis
puc05152
Tuberculosis
puc05160
Hepatitis C
puc05161
Hepatitis B
puc05162
Measles
puc05163
Human cytomegalovirus infection
puc05164
Influenza A
puc05167
Kaposi sarcoma-associated herpesvirus infection
puc05168
Herpes simplex virus 1 infection
puc05169
Epstein-Barr virus infection
puc05170
Human immunodeficiency virus 1 infection
puc05200
Pathways in cancer
puc05210
Colorectal cancer
puc05222
Small cell lung cancer
puc05416
Viral myocarditis
puc05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
puc00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
125929995
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
125929995
04215 Apoptosis - multiple species
125929995
04115 p53 signaling pathway
125929995
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
125929995
09162 Cancer: specific types
05210 Colorectal cancer
125929995
05222 Small cell lung cancer
125929995
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
125929995
05161 Hepatitis B
125929995
05160 Hepatitis C
125929995
05164 Influenza A
125929995
05162 Measles
125929995
05168 Herpes simplex virus 1 infection
125929995
05163 Human cytomegalovirus infection
125929995
05167 Kaposi sarcoma-associated herpesvirus infection
125929995
05169 Epstein-Barr virus infection
125929995
09171 Infectious disease: bacterial
05132 Salmonella infection
125929995
05134 Legionellosis
125929995
05152 Tuberculosis
125929995
09174 Infectious disease: parasitic
05145 Toxoplasmosis
125929995
09164 Neurodegenerative disease
05010 Alzheimer disease
125929995
05012 Parkinson disease
125929995
05014 Amyotrophic lateral sclerosis
125929995
05016 Huntington disease
125929995
05017 Spinocerebellar ataxia
125929995
05020 Prion disease
125929995
05022 Pathways of neurodegeneration - multiple diseases
125929995
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
125929995
05416 Viral myocarditis
125929995
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
125929995
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
125929995
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
125929995
NCBI-ProteinID:
XP_049497569
LinkDB
All DBs
Position
A2:complement(112487685..112490183)
Genome browser
AA seq
105 aa
AA seq
DB search
MGDVEKGKKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTGQAPGFSYTDANKNKGITW
GEETLMEYLENPKKYIPGTKMIFAGIKKAGERADLIAYLKKATKE
NT seq
318 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaagactgggccaaatctccacggtttatttgggcgaaag
acaggccaagcccctgggttttcttacacggatgccaacaagaacaaaggcatcacctgg
ggagaggagacactgatggagtatttggagaatcccaagaagtacatccctggaacaaaa
atgatcttcgctggcattaagaaggcaggggaaagagcagacttgatagcttatctcaaa
aaagctactaaggagtaa
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