Eulemur rufifrons (Bennett's brown lemur): 138376662
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Entry
138376662 CDS
T11398
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2 isoform X1
KO
K15040
voltage-dependent anion channel protein 2
Organism
eruf Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf04020
Calcium signaling pathway
eruf04022
cGMP-PKG signaling pathway
eruf04216
Ferroptosis
eruf04217
Necroptosis
eruf04218
Cellular senescence
eruf04613
Neutrophil extracellular trap formation
eruf04621
NOD-like receptor signaling pathway
eruf04979
Cholesterol metabolism
eruf05010
Alzheimer disease
eruf05012
Parkinson disease
eruf05016
Huntington disease
eruf05017
Spinocerebellar ataxia
eruf05020
Prion disease
eruf05022
Pathways of neurodegeneration - multiple diseases
eruf05166
Human T-cell leukemia virus 1 infection
eruf05208
Chemical carcinogenesis - reactive oxygen species
eruf05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
eruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
138376662 (VDAC2)
04022 cGMP-PKG signaling pathway
138376662 (VDAC2)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
138376662 (VDAC2)
04217 Necroptosis
138376662 (VDAC2)
04218 Cellular senescence
138376662 (VDAC2)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
138376662 (VDAC2)
04621 NOD-like receptor signaling pathway
138376662 (VDAC2)
09154 Digestive system
04979 Cholesterol metabolism
138376662 (VDAC2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
138376662 (VDAC2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
138376662 (VDAC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
138376662 (VDAC2)
05012 Parkinson disease
138376662 (VDAC2)
05016 Huntington disease
138376662 (VDAC2)
05017 Spinocerebellar ataxia
138376662 (VDAC2)
05020 Prion disease
138376662 (VDAC2)
05022 Pathways of neurodegeneration - multiple diseases
138376662 (VDAC2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
138376662 (VDAC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
eruf03029
]
138376662 (VDAC2)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
eruf04040
]
138376662 (VDAC2)
Mitochondrial biogenesis [BR:
eruf03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
138376662 (VDAC2)
Ion channels [BR:
eruf04040
]
Chloride channels
Maxi chloride channel (VDAC)
138376662 (VDAC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
138376662
NCBI-ProteinID:
XP_069317271
LinkDB
All DBs
Position
28:15358247..15378674
Genome browser
AA seq
294 aa
AA seq
DB search
MATYGQTCPRPMCIPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNVNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYQLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq
885 nt
NT seq
+upstream
nt +downstream
nt
atggcgacctacggacagacgtgcccgcggccaatgtgtattcctccatcatatgctgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttggattggtgaaactg
gatgtgaaaacaaagtcatgcagtggtgtggaattctcaacatctggttcatctaacaca
gacactggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagaaaaatggaacactgataacactctgggaacagaaattgcgattgaagac
cagatttgtcaaggtttgaaactgacatttgatactaccttctcacccaacacaggaaag
aaaagtggtaaaatcaagtcctcttacaagagggagtgtataaaccttggttgtgatgtt
gactttgattttgctggacccgcaatccacggttcagctgtctttggttatgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgacaaggaataacttt
gctgtgggctacaggactggtgatttccagctacacactaatgtcaatgatgggacagaa
tttggaggatcaatttatcagaaagtatgtgaagatcttgatacttcggtaaaccttgct
tggacatcaggtaccaactgcactcgatttggcattgcagctaaatatcagttggatccc
actgcttccatttctgcaaaagtcaacaactctagtttaattggagtgggctacactcaa
actctgaggcctggtgtgaagcttacactgtctgctctggtagatgggaagagcattaat
gctggaggccacaaacttgggcttgccctggagttggaggcttaa
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