KEGG   Neogale vison (American mink): 122900317
Entry
122900317         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
    122900317
   04022 cGMP-PKG signaling pathway
    122900317
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    122900317
   04218 Cellular senescence
    122900317
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    122900317
   04621 NOD-like receptor signaling pathway
    122900317
  09154 Digestive system
   04979 Cholesterol metabolism
    122900317
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122900317
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122900317
   05164 Influenza A
    122900317
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122900317
   05012 Parkinson disease
    122900317
   05014 Amyotrophic lateral sclerosis
    122900317
   05016 Huntington disease
    122900317
   05017 Spinocerebellar ataxia
    122900317
   05020 Prion disease
    122900317
   05022 Pathways of neurodegeneration - multiple diseases
    122900317
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122900317
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:nvs03029]
    122900317
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:nvs04040]
    122900317
Mitochondrial biogenesis [BR:nvs03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    122900317
Ion channels [BR:nvs04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   122900317
SSDB
Motif
Pfam: Porin_3 L_PA-C-like
Other DBs
NCBI-GeneID: 122900317
NCBI-ProteinID: XP_044094831
LinkDB
Position
2:95594515..95596266
AA seq 283 aa
MAVPPTYADLGKPARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGEKNAKIKTGYKR
EHINLGCDVDFDIASPSVRGAVVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETTVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLMLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggccgtgcctcccacgtatgctgatcttggcaaacctgccagggatgtcttcaccaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagactaccaaagtgacgggcagtctggaaacc
aagtacaggtggaccgaatatggtctgacgtttacagagaaatggaacactgacaacacg
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacaggggaaaaaaatgcaaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgcgatgtggatttcgacattgccagtccttcagtccggggt
gctgtggtgctgggctatgaaggctggctggctggctaccagatgaattttgagactgcg
aagtctcgagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctc
cacactaacgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccactgtcaatctggcctggactgcaggaaatagtaacactcgctttgga
atagcagccaaatatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgatgctatca
gctctgctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa

DBGET integrated database retrieval system