KEGG   Oryctolagus cuniculus (rabbit): 100349506
Entry
100349506         CDS       T03373                                 
Name
(RefSeq) LOW QUALITY PROTEIN: voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu04621  NOD-like receptor signaling pathway
ocu04979  Cholesterol metabolism
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05014  Amyotrophic lateral sclerosis
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100349506
   04022 cGMP-PKG signaling pathway
    100349506
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100349506
   04218 Cellular senescence
    100349506
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100349506
   04621 NOD-like receptor signaling pathway
    100349506
  09154 Digestive system
   04979 Cholesterol metabolism
    100349506
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100349506
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100349506
   05164 Influenza A
    100349506
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100349506
   05012 Parkinson disease
    100349506
   05014 Amyotrophic lateral sclerosis
    100349506
   05016 Huntington disease
    100349506
   05017 Spinocerebellar ataxia
    100349506
   05020 Prion disease
    100349506
   05022 Pathways of neurodegeneration - multiple diseases
    100349506
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100349506
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100349506
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100349506
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100349506
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100349506
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100349506
NCBI-ProteinID: XP_051710262
LinkDB
Position
12:28453080..28454788
AA seq 276 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKXSSGSANTETTKVTGSLETKYRWTEY
GLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGEKNAKIKTGYKREHINLGC
DVDFDIAGPSIRGALVLGYEGWLADYQMNFETAKSRVTQSNFAVGYKTDEFQLHTNVNDG
TEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNSSLIGLGY
TQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 831 nt   +upstreamnt  +downstreamnt
atggctgtacctcccacgtatgccgatcttggcaaatctgccagggatgtcttcaccaag
ggctacggatttggcttaataaagcttgatttgaaaacaaaancaagctcaggctcagcc
aacactgagaccaccaaagtgacgggcagtctggaaaccaagtacaggtggaccgagtat
gggctgacgtttacggagaaatggaacaccgacaacacgctgggcaccgagatcaccgtg
gaagaccagcttgcacgtggactgaagctgaccttcgattcctccttctcgcctaacact
ggggaaaaaaatgctaaaatcaagacaggctacaagcgggagcacatcaacctgggctgc
gacgtggatttcgacatcgctgggccctccatccggggcgctctggtgctgggttacgag
ggctggctggctgactaccagatgaactttgagactgccaagtcccgagtcacccagagc
aactttgccgtcggctacaagaccgacgaattccagctccacactaatgtgaacgatgga
acggagtttggcggctccatttaccagaaggtgaacaagaagctggagacggccgtcaat
cttgcctggacagcaggaaacagtaacactcgctttggaatagcagccaagtatcagatc
gaccctgacgcctgcttctcggcaaaagtgaacaactccagcctgataggattaggatac
actcagaccctaaagccaggtatcaaactgacgctctcagctctgctggatggcaagaac
gtcaacgctggcggccacaagcttggtctaggactggagtttcaggcataa

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