Equus przewalskii (Przewalski's horse): 103560633
Help
Entry
103560633 CDS
T04644
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2
KO
K15040
voltage-dependent anion channel protein 2
Organism
epz
Equus przewalskii (Przewalski's horse)
Pathway
epz04020
Calcium signaling pathway
epz04022
cGMP-PKG signaling pathway
epz04216
Ferroptosis
epz04217
Necroptosis
epz04218
Cellular senescence
epz04613
Neutrophil extracellular trap formation
epz04621
NOD-like receptor signaling pathway
epz04979
Cholesterol metabolism
epz05010
Alzheimer disease
epz05012
Parkinson disease
epz05016
Huntington disease
epz05017
Spinocerebellar ataxia
epz05020
Prion disease
epz05022
Pathways of neurodegeneration - multiple diseases
epz05166
Human T-cell leukemia virus 1 infection
epz05208
Chemical carcinogenesis - reactive oxygen species
epz05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
epz00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
103560633 (VDAC2)
04022 cGMP-PKG signaling pathway
103560633 (VDAC2)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
103560633 (VDAC2)
04217 Necroptosis
103560633 (VDAC2)
04218 Cellular senescence
103560633 (VDAC2)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
103560633 (VDAC2)
04621 NOD-like receptor signaling pathway
103560633 (VDAC2)
09154 Digestive system
04979 Cholesterol metabolism
103560633 (VDAC2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
103560633 (VDAC2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
103560633 (VDAC2)
09164 Neurodegenerative disease
05010 Alzheimer disease
103560633 (VDAC2)
05012 Parkinson disease
103560633 (VDAC2)
05016 Huntington disease
103560633 (VDAC2)
05017 Spinocerebellar ataxia
103560633 (VDAC2)
05020 Prion disease
103560633 (VDAC2)
05022 Pathways of neurodegeneration - multiple diseases
103560633 (VDAC2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
103560633 (VDAC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
epz03029
]
103560633 (VDAC2)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
epz04040
]
103560633 (VDAC2)
Mitochondrial biogenesis [BR:
epz03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
103560633 (VDAC2)
Ion channels [BR:
epz04040
]
Chloride channels
Maxi chloride channel (VDAC)
103560633 (VDAC2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
103560633
NCBI-ProteinID:
XP_008533054
LinkDB
All DBs
Position
1:62810226..62826697
Genome browser
AA seq
294 aa
AA seq
DB search
MATCGQSCPRPMCVPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNVNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYQLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq
885 nt
NT seq
+upstream
nt +downstream
nt
atggcgacctgcggccagagctgcccgcggccaatgtgtgttcctccatcatatgctgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttggtttggtgaaactg
gatgtgaaaacaaagtcatgcagtggtgtggaattttcaacatctggttcatctaataca
gacactggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagaaaaatggaacactgataacactctgggaacagaaatcgcaattgaagac
cagatttgtcaaggtttgaaactgacatttgataccaccttttcaccaaacacgggaaag
aaaagtggtaaaatcaagtcttcttacaagagggagtgtataaaccttggttgtgatgtt
gactttgattttgctggacctgcaatccatggttcagctgtctttggttatgaaggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgacaaggaataacttt
gcagtaggctacaggactggggacttccagctgcacactaatgtcaatgatgggacagaa
tttggaggatcaatttatcagaaagtatgtgaagatcttgacacttcagtaaaccttgct
tggacatcaggtaccaactgcactcgctttggcattgcagctaaatatcagttggatcct
actgcttccatttctgcaaaagtcaacaactctagtttgattggagtcggctatactcag
actctgaggcctggtgtgaagcttacgctgtctgctctggtagacgggaagagcattaat
gctggaggccacaaacttgggcttgccctggagttggaggcttaa
DBGET
integrated database retrieval system
