KEGG   Mustela lutreola (European mink): 131832988
Entry
131832988         CDS       T09578                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 3-like
  KO
K15041  voltage-dependent anion channel protein 3
Organism
mlk  Mustela lutreola (European mink)
Pathway
mlk04020  Calcium signaling pathway
mlk04022  cGMP-PKG signaling pathway
mlk04216  Ferroptosis
mlk04217  Necroptosis
mlk04218  Cellular senescence
mlk04613  Neutrophil extracellular trap formation
mlk04621  NOD-like receptor signaling pathway
mlk04979  Cholesterol metabolism
mlk05010  Alzheimer disease
mlk05012  Parkinson disease
mlk05016  Huntington disease
mlk05017  Spinocerebellar ataxia
mlk05020  Prion disease
mlk05022  Pathways of neurodegeneration - multiple diseases
mlk05161  Hepatitis B
mlk05166  Human T-cell leukemia virus 1 infection
mlk05203  Viral carcinogenesis
mlk05208  Chemical carcinogenesis - reactive oxygen species
mlk05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mlk00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    131832988
   04022 cGMP-PKG signaling pathway
    131832988
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    131832988
   04217 Necroptosis
    131832988
   04218 Cellular senescence
    131832988
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    131832988
   04621 NOD-like receptor signaling pathway
    131832988
  09154 Digestive system
   04979 Cholesterol metabolism
    131832988
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    131832988
   05203 Viral carcinogenesis
    131832988
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    131832988
   05161 Hepatitis B
    131832988
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    131832988
   05012 Parkinson disease
    131832988
   05016 Huntington disease
    131832988
   05017 Spinocerebellar ataxia
    131832988
   05020 Prion disease
    131832988
   05022 Pathways of neurodegeneration - multiple diseases
    131832988
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    131832988
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mlk03029]
    131832988
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mlk04040]
    131832988
Mitochondrial biogenesis [BR:mlk03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    131832988
Ion channels [BR:mlk04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   131832988
SSDB
Motif
Pfam: Porin_3 Gp44_C
Other DBs
NCBI-GeneID: 131832988
NCBI-ProteinID: XP_059032215
LinkDB
Position
6:complement(157719118..157720473)
AA seq 283 aa
MCNTPTHCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVEFPTSGHAYTDTGKASGNLET
KYKIRNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHMNDGTEFGGSIYQKVNKKIETSINLAWTAGSNNTCFGIAAKYKLDYRTSLSAKVNNA
SLIGLGYTQTLRLGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacgccgactcactgtgacctaggaaaggccgcgaaggatgtcttcaataaa
ggatatggatttggcatggtcaaaatagatctgaaaaccaagtcctgtagtggagtggaa
tttcctacttctggtcatgcctacactgatacagggaaagcgtcaggcaatctagagacc
aaatataagatccgtaactatggacttaccttcactcagaaatggaatacagacaatact
cttggaacagaaatctctttggagaataagttggctgaagggttgaaactgactcttgat
accatatttgtaccgaacacaggaaagaagagtggaaaattgaaggcctcgtataaacgg
gattgtttcagtcttggcagtaacgttgatattgatttttctggaccaaccatctatggc
tgggctgtgttagcttttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataatttcgccctgggttacaaggctgcagacttccagctg
cacactcatatgaatgatggcactgaatttggagggtcgatctaccagaaggttaacaag
aagatagaaacgtcaataaaccttgcttggacggccggcagtaacaacacctgttttggc
atcgctgctaaatacaagctggactatagaacttctctgtctgctaaagtaaataatgcc
agcctgatcggactgggttatactcagacccttcgactgggcgtcaaactgaccctgtca
gctttaatcgatggaaagaacttcaatgcaggaggccacaaggttgggttgggatttgaa
ctagaagcttaa

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