KEGG   Rhinolophus hipposideros (lesser horseshoe bat): 308494782
Entry
308494782         CDS       T12007                                 
Symbol
LOC308494782
Name
(RefSeq) non-selective voltage-gated ion channel VDAC2-like
  KO
K15040  voltage-dependent anion channel protein 2
Organism
rhii  Rhinolophus hipposideros (lesser horseshoe bat)
Pathway
rhii04020  Calcium signaling pathway
rhii04022  cGMP-PKG signaling pathway
rhii04216  Ferroptosis
rhii04217  Necroptosis
rhii04218  Cellular senescence
rhii04613  Neutrophil extracellular trap formation
rhii04621  NOD-like receptor signaling pathway
rhii04979  Cholesterol metabolism
rhii05010  Alzheimer disease
rhii05012  Parkinson disease
rhii05016  Huntington disease
rhii05017  Spinocerebellar ataxia
rhii05020  Prion disease
rhii05022  Pathways of neurodegeneration - multiple diseases
rhii05166  Human T-cell leukemia virus 1 infection
rhii05208  Chemical carcinogenesis - reactive oxygen species
rhii05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:rhii00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    308494782 (LOC308494782)
   04022 cGMP-PKG signaling pathway
    308494782 (LOC308494782)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    308494782 (LOC308494782)
   04217 Necroptosis
    308494782 (LOC308494782)
   04218 Cellular senescence
    308494782 (LOC308494782)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    308494782 (LOC308494782)
   04621 NOD-like receptor signaling pathway
    308494782 (LOC308494782)
  09154 Digestive system
   04979 Cholesterol metabolism
    308494782 (LOC308494782)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    308494782 (LOC308494782)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    308494782 (LOC308494782)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    308494782 (LOC308494782)
   05012 Parkinson disease
    308494782 (LOC308494782)
   05016 Huntington disease
    308494782 (LOC308494782)
   05017 Spinocerebellar ataxia
    308494782 (LOC308494782)
   05020 Prion disease
    308494782 (LOC308494782)
   05022 Pathways of neurodegeneration - multiple diseases
    308494782 (LOC308494782)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    308494782 (LOC308494782)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:rhii03029]
    308494782 (LOC308494782)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:rhii04040]
    308494782 (LOC308494782)
Mitochondrial biogenesis [BR:rhii03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    308494782 (LOC308494782)
Ion channels [BR:rhii04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   308494782 (LOC308494782)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 308494782
NCBI-ProteinID: XP_080898829
LinkDB
Position
X:116284000..116285192
AA seq 294 aa
MATYGQSCARPMCIPSSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSDSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDYDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNDNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTICTRFGIAAKHQLDP
TAFISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq 885 nt   +upstreamnt  +downstreamnt
atggcgacctacggacagagctgcgcgcggccaatgtgtattccttcatcatatgctgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttgggttggtgaaactg
gatgtgaaaacaaagtcatgcagtggtgtggaattctcaacatctgattcatctaataca
gacaccggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagagaaatggaacactgataacactctgggaacagaaatcgcaattgaagac
cagatttgtcaaggtttgaaactgacatttgatactaccttttcaccaaacaccggaaag
aaaagtggtaaaatcaagtcttcttacaagagggagtgtataaaccttggttgtgatgtt
gactatgattttgctggacctgcaatccacggttcagctgtctttggttatgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgaccaggaataacttt
gcagtgggctacaggactggagacttccagctacacactaatgacaatgatggaacagaa
tttggaggatcaatttatcagaaagtatgtgaagatcttgacacctcagtaaaccttgcc
tggacatcaggtaccatctgcactcgtttcggcattgcagctaaacatcagttggatccc
actgctttcatttctgcaaaagtcaacaactctagtttaattggagtgggctacactcag
actctgaggcctggtgtgaagcttacactgtctgctctggtagatgggaagagcattaat
gctggaggccacaaacttgggcttgccttggagttggaggcttaa

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