KEGG   Vulpes vulpes (red fox): 112927770
Entry
112927770         CDS       T05911                                 
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2
  KO
K15040  voltage-dependent anion channel protein 2
Organism
vvp  Vulpes vulpes (red fox)
Pathway
vvp04020  Calcium signaling pathway
vvp04022  cGMP-PKG signaling pathway
vvp04216  Ferroptosis
vvp04217  Necroptosis
vvp04218  Cellular senescence
vvp04613  Neutrophil extracellular trap formation
vvp04621  NOD-like receptor signaling pathway
vvp04979  Cholesterol metabolism
vvp05010  Alzheimer disease
vvp05012  Parkinson disease
vvp05016  Huntington disease
vvp05017  Spinocerebellar ataxia
vvp05020  Prion disease
vvp05022  Pathways of neurodegeneration - multiple diseases
vvp05166  Human T-cell leukemia virus 1 infection
vvp05208  Chemical carcinogenesis - reactive oxygen species
vvp05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:vvp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    112927770 (VDAC2)
   04022 cGMP-PKG signaling pathway
    112927770 (VDAC2)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    112927770 (VDAC2)
   04217 Necroptosis
    112927770 (VDAC2)
   04218 Cellular senescence
    112927770 (VDAC2)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    112927770 (VDAC2)
   04621 NOD-like receptor signaling pathway
    112927770 (VDAC2)
  09154 Digestive system
   04979 Cholesterol metabolism
    112927770 (VDAC2)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    112927770 (VDAC2)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    112927770 (VDAC2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112927770 (VDAC2)
   05012 Parkinson disease
    112927770 (VDAC2)
   05016 Huntington disease
    112927770 (VDAC2)
   05017 Spinocerebellar ataxia
    112927770 (VDAC2)
   05020 Prion disease
    112927770 (VDAC2)
   05022 Pathways of neurodegeneration - multiple diseases
    112927770 (VDAC2)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    112927770 (VDAC2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:vvp03029]
    112927770 (VDAC2)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:vvp04040]
    112927770 (VDAC2)
Mitochondrial biogenesis [BR:vvp03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    112927770 (VDAC2)
Ion channels [BR:vvp04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   112927770 (VDAC2)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 112927770
NCBI-ProteinID: XP_025864988
LinkDB
Position
Unknown
AA seq 271 aa
MATYGQSCARPMCVPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVVSVSYLINPD
ESLYNLMYLAHKIAIEDQICQGLKLTFDTTFSPNTGKKSGKIKSSYKRECINLGCDVDFD
FAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNFAVGYRTGDFQLHTNVNDGTEFGG
SIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYQLDPTASISAKVNNSSLIGVGYTQTLR
PGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq 816 nt   +upstreamnt  +downstreamnt
atggcgacctacgggcagagctgcgcgcggccaatgtgtgttcctccatcctatgctgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttgggctggtgaaactg
gatgtgaaaacaaagtcatgcagtggtgtggtgagtgttagctatctaataaatcctgat
gagtctttatataatttgatgtatctggcccacaaaatcgcaattgaagaccagatctgt
caaggtttgaaactgacatttgataccaccttttcaccaaacacgggaaagaaaagtggt
aaaatcaagtcttcttacaagagggagtgtataaaccttggttgtgatgttgactttgat
tttgccggacctgcaatccatggttcagccgtctttggttatgagggctggcttgctggc
taccagatgacttttgatagtgccaaatcaaagctgacaagaaataactttgcagtgggc
tacaggactggggacttccaactgcacactaatgtcaatgacgggacagaatttggagga
tcaatttatcagaaagtatgtgaagatcttgacacttcagtaaaccttgcgtggacatca
ggtaccaactgcactcgctttggcattgcagccaaatatcagttggatcccactgcttcc
atttctgcaaaagtcaacaactctagtttaattggagtgggctacactcagactctgagg
cctggtgtcaagcttacactgtctgccctggtagatgggaagagcattaatgctggaggc
cacaaacttgggcttgccctggagttggaggcttaa

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