KEGG   Leopardus geoffroyi (Geoffroy's cat): 123596914
Entry
123596914         CDS       T10761                                 
Name
(RefSeq) cytochrome c, testis-specific-like
  KO
K08738  cytochrome c
Organism
lgf  Leopardus geoffroyi (Geoffroy's cat)
Pathway
lgf00190  Oxidative phosphorylation
lgf01100  Metabolic pathways
lgf01524  Platinum drug resistance
lgf04115  p53 signaling pathway
lgf04210  Apoptosis
lgf04215  Apoptosis - multiple species
lgf04932  Non-alcoholic fatty liver disease
lgf05010  Alzheimer disease
lgf05012  Parkinson disease
lgf05014  Amyotrophic lateral sclerosis
lgf05016  Huntington disease
lgf05017  Spinocerebellar ataxia
lgf05020  Prion disease
lgf05022  Pathways of neurodegeneration - multiple diseases
lgf05132  Salmonella infection
lgf05134  Legionellosis
lgf05145  Toxoplasmosis
lgf05152  Tuberculosis
lgf05160  Hepatitis C
lgf05161  Hepatitis B
lgf05162  Measles
lgf05163  Human cytomegalovirus infection
lgf05164  Influenza A
lgf05167  Kaposi sarcoma-associated herpesvirus infection
lgf05168  Herpes simplex virus 1 infection
lgf05169  Epstein-Barr virus infection
lgf05170  Human immunodeficiency virus 1 infection
lgf05200  Pathways in cancer
lgf05210  Colorectal cancer
lgf05222  Small cell lung cancer
lgf05416  Viral myocarditis
lgf05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:lgf00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    123596914
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    123596914
   04215 Apoptosis - multiple species
    123596914
   04115 p53 signaling pathway
    123596914
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    123596914
  09162 Cancer: specific types
   05210 Colorectal cancer
    123596914
   05222 Small cell lung cancer
    123596914
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    123596914
   05161 Hepatitis B
    123596914
   05160 Hepatitis C
    123596914
   05164 Influenza A
    123596914
   05162 Measles
    123596914
   05168 Herpes simplex virus 1 infection
    123596914
   05163 Human cytomegalovirus infection
    123596914
   05167 Kaposi sarcoma-associated herpesvirus infection
    123596914
   05169 Epstein-Barr virus infection
    123596914
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    123596914
   05134 Legionellosis
    123596914
   05152 Tuberculosis
    123596914
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    123596914
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    123596914
   05012 Parkinson disease
    123596914
   05014 Amyotrophic lateral sclerosis
    123596914
   05016 Huntington disease
    123596914
   05017 Spinocerebellar ataxia
    123596914
   05020 Prion disease
    123596914
   05022 Pathways of neurodegeneration - multiple diseases
    123596914
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    123596914
   05416 Viral myocarditis
    123596914
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    123596914
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    123596914
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550
Other DBs
NCBI-GeneID: 123596914
NCBI-ProteinID: XP_045331100
LinkDB
Position
C1:complement(166372313..166394179)
AA seq 133 aa
MRLADKEWAPQSCDPSAHWLRADADRRGDAKAGEKIFIQKCAQCHTVEKGGKHKTGPNLW
GLSGPGRKTGQAPGFSFSDANKNRGIIWGKETLIEYLENPKEYIPGTKMVFAGLKKKSER
EDLIQYLKQATSS
NT seq 402 nt   +upstreamnt  +downstreamnt
atgagactggctgacaaggagtgggcaccgcagtcttgtgatccgagcgctcactggtta
cgggccgatgcagatagaaggggagatgctaaagcaggtgagaagatctttattcagaaa
tgtgctcagtgccacacagtggaaaaaggtggaaaacacaagactggtccaaacctctgg
ggcctttctggccctggacgaaaaacaggacaagcaccaggattttctttttccgatgct
aacaaaaacagaggtattatctggggaaaggaaactctgatagaatatttagagaatcca
aaggaatatatccctggaactaaaatggtctttgctggtcttaaaaagaagagtgagaga
gaagatcttattcagtatttgaaacaggcaacatcttcatga

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