KEGG   Symphalangus syndactylus (siamang): 129487453
Entry
129487453         CDS       T10134                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 3-like isoform X1
  KO
K15041  voltage-dependent anion channel protein 3
Organism
ssyn  Symphalangus syndactylus (siamang)
Pathway
ssyn04020  Calcium signaling pathway
ssyn04022  cGMP-PKG signaling pathway
ssyn04216  Ferroptosis
ssyn04217  Necroptosis
ssyn04218  Cellular senescence
ssyn04613  Neutrophil extracellular trap formation
ssyn04621  NOD-like receptor signaling pathway
ssyn04979  Cholesterol metabolism
ssyn05010  Alzheimer disease
ssyn05012  Parkinson disease
ssyn05016  Huntington disease
ssyn05017  Spinocerebellar ataxia
ssyn05020  Prion disease
ssyn05022  Pathways of neurodegeneration - multiple diseases
ssyn05161  Hepatitis B
ssyn05166  Human T-cell leukemia virus 1 infection
ssyn05203  Viral carcinogenesis
ssyn05208  Chemical carcinogenesis - reactive oxygen species
ssyn05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ssyn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    129487453
   04022 cGMP-PKG signaling pathway
    129487453
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    129487453
   04217 Necroptosis
    129487453
   04218 Cellular senescence
    129487453
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    129487453
   04621 NOD-like receptor signaling pathway
    129487453
  09154 Digestive system
   04979 Cholesterol metabolism
    129487453
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    129487453
   05203 Viral carcinogenesis
    129487453
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    129487453
   05161 Hepatitis B
    129487453
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    129487453
   05012 Parkinson disease
    129487453
   05016 Huntington disease
    129487453
   05017 Spinocerebellar ataxia
    129487453
   05020 Prion disease
    129487453
   05022 Pathways of neurodegeneration - multiple diseases
    129487453
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    129487453
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ssyn03029]
    129487453
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ssyn04040]
    129487453
Mitochondrial biogenesis [BR:ssyn03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    129487453
Ion channels [BR:ssyn04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   129487453
SSDB
Motif
Pfam: Porin_3 Porin_4
Other DBs
NCBI-GeneID: 129487453
NCBI-ProteinID: XP_055144190
LinkDB
Position
8:complement(17100227..17101259)
AA seq 261 aa
MCKTPTYCDLGKAAEDVFNKGYGFGMVKTDLKTKSCSAVEFSTSDHAYTDRGKASGNLEP
ECKFCIYGLTFTQKRNTDNTLGTETSLENKLAEGLKLSLDTILVPNTGKKSGELKASYKW
DCFSVGSNVDIDFSGPSIYSWAVLVFEGWLAGYQMSFDTAKSKLSQNNFALGYEAADLQL
HTHVNDGTEFGGSIYQKVNEIEMSINLAWTAGSKNTRFGIAAKYKLDCRTSLSAKVNNAS
LIGLGCTQTLRPRVKLTLYQL
NT seq 786 nt   +upstreamnt  +downstreamnt
atgtgtaagacgccaacttactgtgacctgggaaaggctgctgaggatgtcttcaacaaa
ggatatggctttggcatggtgaagacagacctgaaaaccaagtcttgtagtgcagtggag
ttttctacatctgatcatgcttacactgatagagggaaagcatcaggcaacctagaaccc
gaatgtaagttctgcatctatggacttaccttcactcaaaaacggaacacagacaatact
cttgggacagaaacctctttggagaataagttggctgaagggttgaaactgagtcttgat
accatcttggtaccgaacacaggaaagaagagtggggaattgaaggcctcctataaatgg
gattgttttagtgttggcagtaatgttgatatagatttttctggaccaagcatctatagc
tgggctgtgttggtctttgaagggtggcttgccggctatcagatgagttttgacacagcc
aaatccaaattgtcacagaataatttcgccctgggttacgaggctgcagacttacagctg
cacacacatgtgaacgatggcactgaatttggaggttctatctaccagaaggttaatgag
attgaaatgtcaataaaccttgcttggacggctgggagtaagaacacccgttttggcatt
gctgctaagtacaagctggattgtagaacttctctctctgctaaagtaaataatgccagc
ctgattggactgggttgtactcagacccttcgacccagagtcaagttgaccctttatcag
ctttaa

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