KEGG   Myotis yumanensis (Yuma myotis): 139006028
Entry
139006028         CDS       T10762                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
  KO
K15041  voltage-dependent anion channel protein 3
Organism
myum  Myotis yumanensis (Yuma myotis)
Pathway
myum04020  Calcium signaling pathway
myum04022  cGMP-PKG signaling pathway
myum04216  Ferroptosis
myum04217  Necroptosis
myum04218  Cellular senescence
myum04613  Neutrophil extracellular trap formation
myum04621  NOD-like receptor signaling pathway
myum04979  Cholesterol metabolism
myum05010  Alzheimer disease
myum05012  Parkinson disease
myum05016  Huntington disease
myum05017  Spinocerebellar ataxia
myum05020  Prion disease
myum05022  Pathways of neurodegeneration - multiple diseases
myum05161  Hepatitis B
myum05166  Human T-cell leukemia virus 1 infection
myum05203  Viral carcinogenesis
myum05208  Chemical carcinogenesis - reactive oxygen species
myum05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:myum00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    139006028 (VDAC3)
   04022 cGMP-PKG signaling pathway
    139006028 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    139006028 (VDAC3)
   04217 Necroptosis
    139006028 (VDAC3)
   04218 Cellular senescence
    139006028 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    139006028 (VDAC3)
   04621 NOD-like receptor signaling pathway
    139006028 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    139006028 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    139006028 (VDAC3)
   05203 Viral carcinogenesis
    139006028 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    139006028 (VDAC3)
   05161 Hepatitis B
    139006028 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    139006028 (VDAC3)
   05012 Parkinson disease
    139006028 (VDAC3)
   05016 Huntington disease
    139006028 (VDAC3)
   05017 Spinocerebellar ataxia
    139006028 (VDAC3)
   05020 Prion disease
    139006028 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    139006028 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    139006028 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:myum03029]
    139006028 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:myum04040]
    139006028 (VDAC3)
Mitochondrial biogenesis [BR:myum03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    139006028 (VDAC3)
Ion channels [BR:myum04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   139006028 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 139006028
NCBI-ProteinID: XP_070264577
LinkDB
Position
Unknown
AA seq 283 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKICNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTTFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLGFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLAAKVNNA
SLIGLGYTQSLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacttactgtgacctaggaaaggctgccaaggatgtcttcaacaaa
ggatatgggtttggcatggtcaaaatagatctgagaaccaagtcatgtagtggagtggaa
ttttctacttctggtcatgcttatactgacacagggaaagcatcaggcaacctagagaca
aaatataagatctgtaactatggacttacattcacccaaaaatggaacacagacaatact
cttggaacagaaatctcttgggaaaataagttggctgaagggttgaaactgactcttgat
accacatttgtaccgaacacaggaaagaagagtgggaagttgaaggcctcctacaaacgg
gattgtttcagtcttggcagtaatgtggatatagatttttctggcccaaccatctatggc
tgggctgtactaggctttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataattttgccctgggttacaaggctgcagacttccagctg
cacactcatgtgaatgatggcactgaatttggagggtctatctaccagaaggttaatgag
aagattgaaacgtcaataaaccttgcttggacagctggcagtaacaacacccgttttggc
atcgctgctaaatacaagttggattgtagaacttctctagctgctaaagtaaataacgcc
agcctgattggactgggttatactcagagtcttcgaccaggagtcaaactgaccctatca
gctttaatcgacggaaagaacttcaatgcaggaggtcacaaggttgggttgggatttgaa
ctagaagcttaa

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