KEGG   Nannospalax galili (Upper Galilee mountains blind mole rat): 103751785
Entry
103751785         CDS       T03372                                 
Name
(RefSeq) cytochrome c, testis-specific
  KO
K08738  cytochrome c
Organism
ngi  Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi00190  Oxidative phosphorylation
ngi01100  Metabolic pathways
ngi01524  Platinum drug resistance
ngi04115  p53 signaling pathway
ngi04210  Apoptosis
ngi04215  Apoptosis - multiple species
ngi04932  Non-alcoholic fatty liver disease
ngi05010  Alzheimer disease
ngi05012  Parkinson disease
ngi05014  Amyotrophic lateral sclerosis
ngi05016  Huntington disease
ngi05017  Spinocerebellar ataxia
ngi05020  Prion disease
ngi05022  Pathways of neurodegeneration - multiple diseases
ngi05132  Salmonella infection
ngi05134  Legionellosis
ngi05145  Toxoplasmosis
ngi05152  Tuberculosis
ngi05160  Hepatitis C
ngi05161  Hepatitis B
ngi05162  Measles
ngi05163  Human cytomegalovirus infection
ngi05164  Influenza A
ngi05167  Kaposi sarcoma-associated herpesvirus infection
ngi05168  Herpes simplex virus 1 infection
ngi05169  Epstein-Barr virus infection
ngi05170  Human immunodeficiency virus 1 infection
ngi05200  Pathways in cancer
ngi05210  Colorectal cancer
ngi05222  Small cell lung cancer
ngi05416  Viral myocarditis
ngi05417  Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:ngi00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    103751785
 09140 Cellular Processes
  09143 Cell growth and death
   04210 Apoptosis
    103751785
   04215 Apoptosis - multiple species
    103751785
   04115 p53 signaling pathway
    103751785
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103751785
  09162 Cancer: specific types
   05210 Colorectal cancer
    103751785
   05222 Small cell lung cancer
    103751785
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    103751785
   05161 Hepatitis B
    103751785
   05160 Hepatitis C
    103751785
   05164 Influenza A
    103751785
   05162 Measles
    103751785
   05168 Herpes simplex virus 1 infection
    103751785
   05163 Human cytomegalovirus infection
    103751785
   05167 Kaposi sarcoma-associated herpesvirus infection
    103751785
   05169 Epstein-Barr virus infection
    103751785
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    103751785
   05134 Legionellosis
    103751785
   05152 Tuberculosis
    103751785
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    103751785
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103751785
   05012 Parkinson disease
    103751785
   05014 Amyotrophic lateral sclerosis
    103751785
   05016 Huntington disease
    103751785
   05017 Spinocerebellar ataxia
    103751785
   05020 Prion disease
    103751785
   05022 Pathways of neurodegeneration - multiple diseases
    103751785
  09166 Cardiovascular disease
   05417 Lipid and atherosclerosis
    103751785
   05416 Viral myocarditis
    103751785
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    103751785
  09176 Drug resistance: antineoplastic
   01524 Platinum drug resistance
    103751785
SSDB
Motif
Pfam: Cytochrom_C Cytochrome_CBB3 Cytochrom_C550 Dehyd-heme_bind CCP_MauG
Other DBs
NCBI-GeneID: 103751785
NCBI-ProteinID: XP_008853549
UniProt: A0A8C6S0B9
LinkDB
Position
Un
AA seq 105 aa
MGDAEAGKKIFVQKCAQCHTVEKGGKHKTGPNLWGLFGRKTGQVPGFSYTDANKNKGIVW
TEETLMEYLENPKKYIPGTKMIFAGIKKKSEREDLVQYLKEATSS
NT seq 318 nt   +upstreamnt  +downstreamnt
atgggagacgctgaagcaggcaagaagatctttgttcagaaatgtgctcagtgccacaca
gtggagaaaggtggaaagcacaagacgggtccaaatctctggggcctctttggccgaaag
acaggacaagtgccaggattttcttacacggatgcaaacaaaaacaaaggtattgtctgg
acagaagaaactttgatggaatatttggagaacccgaagaaatatatccctggaactaaa
atgatctttgctggtattaaaaagaagagtgagagagaagatcttgttcagtatttgaaa
gaggcaacatcttcatga

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