KEGG   Peromyscus maniculatus bairdii (prairie deer mouse): 102918327
Entry
102918327         CDS       T11302                                 
Name
(RefSeq) cytochrome c, testis-specific
  KO
K08738  cytochrome c
Organism
pmav  Peromyscus maniculatus bairdii (prairie deer mouse)
Pathway
pmav00190  Oxidative phosphorylation
pmav01100  Metabolic pathways
pmav01524  Platinum drug resistance
pmav04115  p53 signaling pathway
pmav04210  Apoptosis
pmav04215  Apoptosis - multiple species
pmav04932  Non-alcoholic fatty liver disease
pmav05010  Alzheimer disease
pmav05012  Parkinson disease
pmav05014  Amyotrophic lateral sclerosis
pmav05016  Huntington disease
pmav05017  Spinocerebellar ataxia
pmav05020  Prion disease
pmav05022  Pathways of neurodegeneration - multiple diseases
pmav05132  Salmonella infection
pmav05134  Legionellosis
pmav05145  Toxoplasmosis
pmav05152  Tuberculosis
pmav05160  Hepatitis C
pmav05161  Hepatitis B
pmav05162  Measles
pmav05163  Human cytomegalovirus infection
pmav05164  Influenza A
pmav05167  Kaposi sarcoma-associated herpesvirus infection
pmav05168  Herpes simplex virus 1 infection
pmav05169  Epstein-Barr virus infection
pmav05170  Human immunodeficiency virus 1 infection
pmav05200  Pathways in cancer
pmav05210  Colorectal cancer
pmav05222  Small cell lung cancer
pmav05416  Viral myocarditis
pmav05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:pmav00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    102918327
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    102918327
   04215 Apoptosis - multiple species
    102918327
   04115 p53 signaling pathway
    102918327
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102918327
  09162 Cancer: specific types
   05210 Colorectal cancer
    102918327
   05222 Small cell lung cancer
    102918327
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    102918327
   05161 Hepatitis B
    102918327
   05160 Hepatitis C
    102918327
   05164 Influenza A
    102918327
   05162 Measles
    102918327
   05168 Herpes simplex virus 1 infection
    102918327
   05163 Human cytomegalovirus infection
    102918327
   05167 Kaposi sarcoma-associated herpesvirus infection
    102918327
   05169 Epstein-Barr virus infection
    102918327
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    102918327
   05134 Legionellosis
    102918327
   05152 Tuberculosis
    102918327
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    102918327
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102918327
   05012 Parkinson disease
    102918327
   05014 Amyotrophic lateral sclerosis
    102918327
   05016 Huntington disease
    102918327
   05017 Spinocerebellar ataxia
    102918327
   05020 Prion disease
    102918327
   05022 Pathways of neurodegeneration - multiple diseases
    102918327
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    102918327
   05416 Viral myocarditis
    102918327
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    102918327
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    102918327
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550
Other DBs
NCBI-GeneID: 102918327
NCBI-ProteinID: XP_006972530
Ensembl: ENSPEMG00000022193
UniProt: A0A6I9KWX0
LinkDB
Position
4:complement(54248853..54257554)
AA seq 105 aa
MGDAEAGKKIFVQKCAQCHTVEKGGKHKTGPNLWGLFGRKTGQAPGFSYTDANKNKGIIW
TEASLMEYLENPKKFIPGTKMIFAGIKKKSEREDLIQYLKRATSS
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggagatgctgaagcaggcaagaagatcttcgttcagaaatgtgctcagtgccacaca
gtggaaaaaggaggaaaacacaagacaggtcccaatctctggggcctttttggccgaaag
acaggccaagccccaggattttcctacactgacgccaacaaaaacaaaggtattatctgg
acagaagcaagtttgatggaatatttggagaacccaaagaaattcatccctggtactaag
atgatctttgctggcataaaaaagaagagcgagagagaagaccttattcagtatttgaaa
cgggccacatcctcatga

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