KEGG   Oryctolagus cuniculus (rabbit): 100008752
Entry
100008752         CDS       T03373                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3
  KO
K15041  voltage-dependent anion channel protein 3
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04216  Ferroptosis
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
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05161  Hepatitis B
ocu05166  Human T-cell leukemia virus 1 infection
ocu05203  Viral carcinogenesis
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
    100008752 (VDAC3)
   04022 cGMP-PKG signaling pathway
    100008752 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    100008752 (VDAC3)
   04217 Necroptosis
    100008752 (VDAC3)
   04218 Cellular senescence
    100008752 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100008752 (VDAC3)
   04621 NOD-like receptor signaling pathway
    100008752 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    100008752 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100008752 (VDAC3)
   05203 Viral carcinogenesis
    100008752 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100008752 (VDAC3)
   05161 Hepatitis B
    100008752 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100008752 (VDAC3)
   05012 Parkinson disease
    100008752 (VDAC3)
   05016 Huntington disease
    100008752 (VDAC3)
   05017 Spinocerebellar ataxia
    100008752 (VDAC3)
   05020 Prion disease
    100008752 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    100008752 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100008752 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100008752 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100008752 (VDAC3)
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100008752 (VDAC3)
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100008752 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100008752
NCBI-ProteinID: NP_001075545
Ensembl: ENSOCUG00000024318
UniProt: Q9TT13
LinkDB
AA seq 283 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNNA
SLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacgtactgtgacctaggaaaggctgccaaggatgtcttcaacaaa
ggatacgggtttggcatggtcaaaatagacctgagaaccaagtcttgtagtggagtggaa
ttttctacttctggtcatgcttacactgatacaggaaaagcgtcaggcaacctagagacc
aaatataaggtctgtaactatggactcaccttcacccagaaatggaacacagacaacact
ctggggacagaaatctctctggagaataagttggctgaaggattgaaactgactcttgac
accatatttgtaccaaacacaggaaagaagagtgggaaattgaaggcctcctataaacgg
gattgttttagtcttggaagtaatgttgatatagatttttctggaccaaccatctatggc
tgggctgtgttggcttttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataattttgccctgggttacaaggctgcagacttccagctg
cacactcatgtaaacgatggcactgaattcggaggctccatctaccagaaggtcaacgag
aagattgaaacgtcaataaacctcgcatggacggctggcagtaacaacacgcgttttggc
atcgcagctaaatacaagctggattgtagaacttctctctctgccaaagtaaataacgcc
agcctgattggactgggttatacgcagacccttcgaccaggagtcaaattgaccctgtcc
gctttaatcgacgggaagaacttcaacgcaggaggccataaggttgggctgggatttgag
ctggaagcctaa

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