KEGG   Neogale vison (American mink): 122904870
Entry
122904870         CDS       T08764                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04020  Calcium signaling pathway
nvs04022  cGMP-PKG signaling pathway
nvs04217  Necroptosis
nvs04218  Cellular senescence
nvs04613  Neutrophil extracellular trap formation
nvs04621  NOD-like receptor signaling pathway
nvs04979  Cholesterol metabolism
nvs05010  Alzheimer disease
nvs05012  Parkinson disease
nvs05014  Amyotrophic lateral sclerosis
nvs05016  Huntington disease
nvs05017  Spinocerebellar ataxia
nvs05020  Prion disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05164  Influenza A
nvs05166  Human T-cell leukemia virus 1 infection
nvs05208  Chemical carcinogenesis - reactive oxygen species
nvs05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    122904870
   04022 cGMP-PKG signaling pathway
    122904870
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    122904870
   04218 Cellular senescence
    122904870
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    122904870
   04621 NOD-like receptor signaling pathway
    122904870
  09154 Digestive system
   04979 Cholesterol metabolism
    122904870
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122904870
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122904870
   05164 Influenza A
    122904870
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122904870
   05012 Parkinson disease
    122904870
   05014 Amyotrophic lateral sclerosis
    122904870
   05016 Huntington disease
    122904870
   05017 Spinocerebellar ataxia
    122904870
   05020 Prion disease
    122904870
   05022 Pathways of neurodegeneration - multiple diseases
    122904870
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122904870
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:nvs03029]
    122904870
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:nvs04040]
    122904870
Mitochondrial biogenesis [BR:nvs03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    122904870
Ion channels [BR:nvs04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   122904870
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 122904870
NCBI-ProteinID: XP_044102069
LinkDB
Position
4:complement(171756260..171758071)
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLACGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGAVVLGYEGWLAGYQMNFETAKSLVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggccgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagactaccaaagtgacgggcagtctggaaacc
aagtacaggtggaccgaatatggtctgacgtttacagagaaatggaacactgacaacacg
ctaggcacagagatcactgtggaagatcagcttgcatgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgcaaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgcgatgtggatttcgacattgccggtccttcagtccggggt
gctgtggtgctgggctatgaaggctggctggctggctaccagatgaattttgagactgcg
aagtctctagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctc
cacactaacgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgtcaatctggcctggactgcaggaaatagtaacactcgctttgga
atagcagccaaatatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatca
gctctgctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa

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