KEGG   Alexandromys fortis (reed vole): 126510981
Entry
126510981         CDS       T08493                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
mfot  Alexandromys fortis (reed vole)
Pathway
mfot04020  Calcium signaling pathway
mfot04022  cGMP-PKG signaling pathway
mfot04217  Necroptosis
mfot04218  Cellular senescence
mfot04613  Neutrophil extracellular trap formation
mfot04621  NOD-like receptor signaling pathway
mfot04979  Cholesterol metabolism
mfot05010  Alzheimer disease
mfot05012  Parkinson disease
mfot05014  Amyotrophic lateral sclerosis
mfot05016  Huntington disease
mfot05017  Spinocerebellar ataxia
mfot05020  Prion disease
mfot05022  Pathways of neurodegeneration - multiple diseases
mfot05164  Influenza A
mfot05166  Human T-cell leukemia virus 1 infection
mfot05208  Chemical carcinogenesis - reactive oxygen species
mfot05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mfot00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    126510981
   04022 cGMP-PKG signaling pathway
    126510981
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    126510981
   04218 Cellular senescence
    126510981
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    126510981
   04621 NOD-like receptor signaling pathway
    126510981
  09154 Digestive system
   04979 Cholesterol metabolism
    126510981
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    126510981
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    126510981
   05164 Influenza A
    126510981
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    126510981
   05012 Parkinson disease
    126510981
   05014 Amyotrophic lateral sclerosis
    126510981
   05016 Huntington disease
    126510981
   05017 Spinocerebellar ataxia
    126510981
   05020 Prion disease
    126510981
   05022 Pathways of neurodegeneration - multiple diseases
    126510981
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    126510981
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mfot03029]
    126510981
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mfot04040]
    126510981
Mitochondrial biogenesis [BR:mfot03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    126510981
Ion channels [BR:mfot04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   126510981
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 126510981
NCBI-ProteinID: XP_050013755
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVNGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETSKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQVDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNINAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacatatgctgatcttggcaagtctgccagggatgtcttcaccaag
ggctatggctttggcttaataaaacttgatttgaaaacgaagtcggagaatggattggaa
tttaccagctcaggctccgccaacacagagaccaccaaagtgaacggcagtctggaaacc
aagtatcgatggactgagtatggcctgacgtttacagaaaagtggaacacagacaacacc
ctgggtaccgagatcaccgtggaagaccagctcgcgcgtgggctgaagctgaccttcgac
tcatccttctcacctaatactgggaaaaaaaatgctaaaatcaagacagggtacaagagg
gagcatatcaacctgggctgtgatgtggactttgacatcgctgggccctcgatccggggt
gccctggtacttggctatgagggctggctagcaggctaccaaatgaattttgagacttcc
aagtcccgagtgacccagagcaactttgcagttggctacaagacggatgaattccagctt
catactaatgtgaatgatgggacggagtttggtggctccatctaccaaaaggtgaacaag
aagttggagactgctgtcaatctcgcctggacagcggggaatagtaacactcgctttggg
atagcagccaagtaccaggtcgaccctgacgcctgtttttcggccaaagtgaacaactct
agcctgatcggcttagggtacactcagaccctcaagccaggtatcaagctgacgctgtca
gctctgctggatggcaagaacatcaacgcaggtggccacaagcttggtctaggactagaa
tttcaagcataa

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