Prionailurus viverrinus (fishing cat): 125170217
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Entry
125170217 CDS
T09889
Name
(RefSeq) cytochrome c-like isoform X1
KO
K08738
cytochrome c
Organism
pviv
Prionailurus viverrinus (fishing cat)
Pathway
pviv00190
Oxidative phosphorylation
pviv01100
Metabolic pathways
pviv01524
Platinum drug resistance
pviv04115
p53 signaling pathway
pviv04210
Apoptosis
pviv04215
Apoptosis - multiple species
pviv04932
Non-alcoholic fatty liver disease
pviv05010
Alzheimer disease
pviv05012
Parkinson disease
pviv05014
Amyotrophic lateral sclerosis
pviv05016
Huntington disease
pviv05017
Spinocerebellar ataxia
pviv05020
Prion disease
pviv05022
Pathways of neurodegeneration - multiple diseases
pviv05132
Salmonella infection
pviv05134
Legionellosis
pviv05145
Toxoplasmosis
pviv05152
Tuberculosis
pviv05160
Hepatitis C
pviv05161
Hepatitis B
pviv05162
Measles
pviv05163
Human cytomegalovirus infection
pviv05164
Influenza A
pviv05167
Kaposi sarcoma-associated herpesvirus infection
pviv05168
Herpes simplex virus 1 infection
pviv05169
Epstein-Barr virus infection
pviv05170
Human immunodeficiency virus 1 infection
pviv05200
Pathways in cancer
pviv05210
Colorectal cancer
pviv05222
Small cell lung cancer
pviv05416
Viral myocarditis
pviv05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
pviv00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
125170217
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
125170217
04215 Apoptosis - multiple species
125170217
04115 p53 signaling pathway
125170217
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
125170217
09162 Cancer: specific types
05210 Colorectal cancer
125170217
05222 Small cell lung cancer
125170217
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
125170217
05161 Hepatitis B
125170217
05160 Hepatitis C
125170217
05164 Influenza A
125170217
05162 Measles
125170217
05168 Herpes simplex virus 1 infection
125170217
05163 Human cytomegalovirus infection
125170217
05167 Kaposi sarcoma-associated herpesvirus infection
125170217
05169 Epstein-Barr virus infection
125170217
09171 Infectious disease: bacterial
05132 Salmonella infection
125170217
05134 Legionellosis
125170217
05152 Tuberculosis
125170217
09174 Infectious disease: parasitic
05145 Toxoplasmosis
125170217
09164 Neurodegenerative disease
05010 Alzheimer disease
125170217
05012 Parkinson disease
125170217
05014 Amyotrophic lateral sclerosis
125170217
05016 Huntington disease
125170217
05017 Spinocerebellar ataxia
125170217
05020 Prion disease
125170217
05022 Pathways of neurodegeneration - multiple diseases
125170217
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
125170217
05416 Viral myocarditis
125170217
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
125170217
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
125170217
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
125170217
NCBI-ProteinID:
XP_047722560
LinkDB
All DBs
Position
B4:complement(79987588..79994177)
Genome browser
AA seq
145 aa
AA seq
DB search
MKLNVYSSDIGLEVLSGWRAGHPAWEQAPSFRAQPKSDLKMGDVEKGKKIFVQKCAQCHT
VEKGGKHKTGPNLHGLFGRKTGQAPGLSYTDANKNKGITWGEETLMEYLENPKKYVPGTK
MIFAGIKKAGERANLIAYLKKATKE
NT seq
438 nt
NT seq
+upstream
nt +downstream
nt
atgaagctcaatgtctacagttctgacataggcttagaagtactatcggggtggagagct
ggacatccggcttgggagcaggcaccttcgtttcgcgcgcaaccaaagagcgatttaaaa
atgggtgatgttgagaagggcaagaagatttttgttcagaagtgtgcccagtgccatact
gtggaaaagggaggcaagcacaagactggaccaaatctccatggtttatttgggcgaaaa
acaggtcaagcccctgggttgtcttacacagatgccaacaagaacaaaggtatcacctgg
ggagaggagacattgatggagtatttggagaatcccaagaagtacgtccctggaacaaaa
atgatcttcgctggcattaagaaggcaggggaaagagcgaacttgatagcttatctcaaa
aaagctactaaggaataa
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integrated database retrieval system