Hipposideros armiger (great roundleaf bat): 109372707
Help
Entry
109372707 CDS
T04661
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2 isoform X1
KO
K15040
voltage-dependent anion channel protein 2
Organism
hai
Hipposideros armiger (great roundleaf bat)
Pathway
hai04020
Calcium signaling pathway
hai04022
cGMP-PKG signaling pathway
hai04216
Ferroptosis
hai04217
Necroptosis
hai04218
Cellular senescence
hai04613
Neutrophil extracellular trap formation
hai04621
NOD-like receptor signaling pathway
hai04979
Cholesterol metabolism
hai05010
Alzheimer disease
hai05012
Parkinson disease
hai05016
Huntington disease
hai05017
Spinocerebellar ataxia
hai05020
Prion disease
hai05022
Pathways of neurodegeneration - multiple diseases
hai05166
Human T-cell leukemia virus 1 infection
hai05208
Chemical carcinogenesis - reactive oxygen species
hai05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
hai00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
109372707 (VDAC2)
04022 cGMP-PKG signaling pathway
109372707 (VDAC2)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
109372707 (VDAC2)
04217 Necroptosis
109372707 (VDAC2)
04218 Cellular senescence
109372707 (VDAC2)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
109372707 (VDAC2)
04621 NOD-like receptor signaling pathway
109372707 (VDAC2)
09154 Digestive system
04979 Cholesterol metabolism
109372707 (VDAC2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
109372707 (VDAC2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
109372707 (VDAC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
109372707 (VDAC2)
05012 Parkinson disease
109372707 (VDAC2)
05016 Huntington disease
109372707 (VDAC2)
05017 Spinocerebellar ataxia
109372707 (VDAC2)
05020 Prion disease
109372707 (VDAC2)
05022 Pathways of neurodegeneration - multiple diseases
109372707 (VDAC2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
109372707 (VDAC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hai03029
]
109372707 (VDAC2)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
hai04040
]
109372707 (VDAC2)
Mitochondrial biogenesis [BR:
hai03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
109372707 (VDAC2)
Ion channels [BR:
hai04040
]
Chloride channels
Maxi chloride channel (VDAC)
109372707 (VDAC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
109372707
NCBI-ProteinID:
XP_019481678
UniProt:
A0A8B7Q2E7
LinkDB
All DBs
Position
Unknown
AA seq
294 aa
AA seq
DB search
MATYGQSCARPMCIPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNVNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYKLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq
885 nt
NT seq
+upstream
nt +downstream
nt
atggcgacttacggacagagctgcgcgcggccaatgtgtattcctccatcatatgctgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttgggttggtgaaattg
gatgtgaaaacaaagtcatgcagtggtgtggaattctcaacatcaggttcatctaataca
gacactggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggcctg
actttcacagagaaatggaacactgataacactctgggaacagaaatcgcaattgaagac
cagatttgtcaaggtttgaagctgacatttgataccaccttttctccaaacacaggaaag
aaaagtggtaaaatcaagtcttcttacaagagggagtgtataaacctcggttgtgatgtt
gactttgattttgctggacctgcaatccatgggtcagctgtctttggttatgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgaccaggaataacttt
gcagtgggctacaggactggagatttccagctacacactaatgtcaatgatggaacagaa
tttggaggatcaatttatcagaaagtatgtgaagatcttgacacttcagtaaaccttgct
tggacatcaggtaccaactgcactcggttcggcattgcagctaaatataagttggatccc
actgcttccatttcggcaaaagtcaacaactctagtttaattggagtgggctacactcag
actctgaggcctggtgtgaagcttacactgtctgctctggtagatgggaagagcattaat
gctggaggccacaaacttgggcttgccctggagttggaggcttaa
DBGET
integrated database retrieval system