KEGG   Oryctolagus cuniculus (rabbit): 100353673
Entry
100353673         CDS       T03373                                 
Name
(RefSeq) cytochrome c, testis-specific isoform X1
  KO
K08738  cytochrome c
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu00190  Oxidative phosphorylation
ocu01100  Metabolic pathways
ocu01524  Platinum drug resistance
ocu04115  p53 signaling pathway
ocu04210  Apoptosis
ocu04215  Apoptosis - multiple species
ocu04932  Non-alcoholic fatty liver disease
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05014  Amyotrophic lateral sclerosis
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05132  Salmonella infection
ocu05134  Legionellosis
ocu05145  Toxoplasmosis
ocu05152  Tuberculosis
ocu05160  Hepatitis C
ocu05161  Hepatitis B
ocu05162  Measles
ocu05163  Human cytomegalovirus infection
ocu05164  Influenza A
ocu05167  Kaposi sarcoma-associated herpesvirus infection
ocu05168  Herpes simplex virus 1 infection
ocu05169  Epstein-Barr virus infection
ocu05170  Human immunodeficiency virus 1 infection
ocu05200  Pathways in cancer
ocu05210  Colorectal cancer
ocu05222  Small cell lung cancer
ocu05416  Viral myocarditis
ocu05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    100353673
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    100353673
   04215 Apoptosis - multiple species
    100353673
   04115 p53 signaling pathway
    100353673
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100353673
  09162 Cancer: specific types
   05210 Colorectal cancer
    100353673
   05222 Small cell lung cancer
    100353673
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    100353673
   05161 Hepatitis B
    100353673
   05160 Hepatitis C
    100353673
   05164 Influenza A
    100353673
   05162 Measles
    100353673
   05168 Herpes simplex virus 1 infection
    100353673
   05163 Human cytomegalovirus infection
    100353673
   05167 Kaposi sarcoma-associated herpesvirus infection
    100353673
   05169 Epstein-Barr virus infection
    100353673
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    100353673
   05134 Legionellosis
    100353673
   05152 Tuberculosis
    100353673
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    100353673
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100353673
   05012 Parkinson disease
    100353673
   05014 Amyotrophic lateral sclerosis
    100353673
   05016 Huntington disease
    100353673
   05017 Spinocerebellar ataxia
    100353673
   05020 Prion disease
    100353673
   05022 Pathways of neurodegeneration - multiple diseases
    100353673
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    100353673
   05416 Viral myocarditis
    100353673
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    100353673
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    100353673
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550
Other DBs
NCBI-GeneID: 100353673
NCBI-ProteinID: XP_002712354
Ensembl: ENSOCUG00000025342
UniProt: G1TTC7
LinkDB
Position
7:55807025..55819538
AA seq 153 aa
MADQTCECHRGPAAEPPPSNSGRGLPPGRGTGEEESRATGPVVPLQSKMGDAETGKKIFI
QKCAQCHTVEKGGKHKTGPNLWGLFGRKTGQAQGFSYSDANKNKGIVWGEDTLMEYLENP
KKYIPGTKMVFAGLKKKTEREDLIQYLKQATSS
NT seq 462 nt   +upstreamnt  +downstreamnt
atggctgaccagacctgcgagtgtcatcgaggccctgctgcagaaccaccaccatcgaac
tcggggcgcggactcccgcctggccgcggcacaggggaggaggagagcagagctactggc
cctgtggttcctctgcagagcaaaatgggagatgctgaaacaggcaagaagatctttatt
cagaaatgtgctcagtgccacacagtagaaaaaggtggaaaacacaagactggtccaaat
ctctggggtctctttggccgaaaaacaggacaagcacaaggattctcttattctgatgca
aacaaaaacaaaggtattgtctggggagaagatactctgatggaatatttggagaaccca
aagaaatatatccctggaactaaaatggtctttgctggtcttaaaaagaagactgagaga
gaagatcttattcaatatttgaaacaggccacgtcttcatga

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