KEGG   Peromyscus leucopus (white-footed mouse): 114691928
Entry
114691928         CDS       T07241                                 
Name
(RefSeq) LOW QUALITY PROTEIN: voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
pleu  Peromyscus leucopus (white-footed mouse)
Pathway
pleu04020  Calcium signaling pathway
pleu04022  cGMP-PKG signaling pathway
pleu04217  Necroptosis
pleu04218  Cellular senescence
pleu04613  Neutrophil extracellular trap formation
pleu04621  NOD-like receptor signaling pathway
pleu04979  Cholesterol metabolism
pleu05010  Alzheimer disease
pleu05012  Parkinson disease
pleu05014  Amyotrophic lateral sclerosis
pleu05016  Huntington disease
pleu05017  Spinocerebellar ataxia
pleu05020  Prion disease
pleu05022  Pathways of neurodegeneration - multiple diseases
pleu05164  Influenza A
pleu05166  Human T-cell leukemia virus 1 infection
pleu05208  Chemical carcinogenesis - reactive oxygen species
pleu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:pleu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    114691928
   04022 cGMP-PKG signaling pathway
    114691928
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    114691928
   04218 Cellular senescence
    114691928
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    114691928
   04621 NOD-like receptor signaling pathway
    114691928
  09154 Digestive system
   04979 Cholesterol metabolism
    114691928
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    114691928
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    114691928
   05164 Influenza A
    114691928
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    114691928
   05012 Parkinson disease
    114691928
   05014 Amyotrophic lateral sclerosis
    114691928
   05016 Huntington disease
    114691928
   05017 Spinocerebellar ataxia
    114691928
   05020 Prion disease
    114691928
   05022 Pathways of neurodegeneration - multiple diseases
    114691928
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    114691928
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:pleu03029]
    114691928
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:pleu04040]
    114691928
Mitochondrial biogenesis [BR:pleu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    114691928
Ion channels [BR:pleu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   114691928
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 114691928
NCBI-ProteinID: XP_037065603
LinkDB
Position
12:41041943..41043367
AA seq 283 aa
MAVSPTYADLGKSARDVFTKGYGFGLLKLDLKTKSENGLELTSSGSANTETTKVNGSLET
KYRWTEYGLMLTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSTNTGKKNAKIKTGYKR
EHINLGCDVDFDIARPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQTVNKKLETAVNLAWTAGNSNTRLGIAAKYQVDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLVGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgtctcccacatatgctgatcttggcaagtctgccagggatgtcttcaccaag
ggctacggctttggcttactaaaacttgatttgaaaacgaagtctgagaatggattggaa
ttgaccagctcaggctccgccaacacagagaccaccaaagtgaacggcagcctggaaacc
aagtacagatggactgagtacgggctgatgttgacagagaagtggaacacagacaacacc
ctgggtaccgagatcaccgtggaagaccagctcgcgcgtggactgaagctgacctttgat
tcatccttctcgactaacactgggaaaaaaaatgctaaaatcaagacagggtacaagagg
gagcatatcaacctgggctgtgatgtggactttgacatcgcccggccctcgatccgtggc
gctctggtgcttggctatgagggttggctggctggctaccagatgaattttgagaccgcg
aagtcccgagtgacccagagcaactttgccgttggctacaagacggacgaattccagctt
catactaatgtgaacgatgggacagagtttggtggctccatttatcagacggtgaacaag
aagttggagaccgctgttaatctcgcctggacagcaggaaacagtaacactcgcttagga
atagcagccaagtatcaggtcgaccctgatgcctgcttttcggccaaagtgaacaactct
agcctcatcggcttagggtacactcagaccctaaagccaggtatcaaactgaccctgtcg
gctctgctggttggcaagaacgtcaatgcgggtggccacaagcttggtctaggactggaa
tttcaagcataa

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