Nannospalax galili (Upper Galilee mountains blind mole rat): 103747445
Help
Entry
103747445 CDS
T03372
Symbol
Vdac2
Name
(RefSeq) voltage dependent anion channel 2
KO
K15040
voltage-dependent anion channel protein 2
Organism
ngi
Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi04020
Calcium signaling pathway
ngi04022
cGMP-PKG signaling pathway
ngi04216
Ferroptosis
ngi04217
Necroptosis
ngi04218
Cellular senescence
ngi04613
Neutrophil extracellular trap formation
ngi04621
NOD-like receptor signaling pathway
ngi04979
Cholesterol metabolism
ngi05010
Alzheimer disease
ngi05012
Parkinson disease
ngi05016
Huntington disease
ngi05017
Spinocerebellar ataxia
ngi05020
Prion disease
ngi05022
Pathways of neurodegeneration - multiple diseases
ngi05166
Human T-cell leukemia virus 1 infection
ngi05208
Chemical carcinogenesis - reactive oxygen species
ngi05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
ngi00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
103747445 (Vdac2)
04022 cGMP-PKG signaling pathway
103747445 (Vdac2)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
103747445 (Vdac2)
04217 Necroptosis
103747445 (Vdac2)
04218 Cellular senescence
103747445 (Vdac2)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
103747445 (Vdac2)
04621 NOD-like receptor signaling pathway
103747445 (Vdac2)
09154 Digestive system
04979 Cholesterol metabolism
103747445 (Vdac2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
103747445 (Vdac2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
103747445 (Vdac2)
09164 Neurodegenerative disease
05010 Alzheimer disease
103747445 (Vdac2)
05012 Parkinson disease
103747445 (Vdac2)
05016 Huntington disease
103747445 (Vdac2)
05017 Spinocerebellar ataxia
103747445 (Vdac2)
05020 Prion disease
103747445 (Vdac2)
05022 Pathways of neurodegeneration - multiple diseases
103747445 (Vdac2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
103747445 (Vdac2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
ngi03029
]
103747445 (Vdac2)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
ngi04040
]
103747445 (Vdac2)
Mitochondrial biogenesis [BR:
ngi03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
103747445 (Vdac2)
Ion channels [BR:
ngi04040
]
Chloride channels
Maxi chloride channel (VDAC)
103747445 (Vdac2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
103747445
NCBI-ProteinID:
XP_008848118
UniProt:
A0A8C6RJJ7
LinkDB
All DBs
Position
Un
AA seq
294 aa
AA seq
DB search
MADCVRTCARPMCIPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRSNF
AVGYRTGDFQLHTNVNNGTEFGGSIYQKVCENFDTSVNLAWTSGTNCTRFGIAAKYQLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSFNAGGHKLGLALELEA
NT seq
885 nt
NT seq
+upstream
nt +downstream
nt
atggcagactgtgtacggacctgcgcgcggccaatgtgtatccctccatcatatgctgac
cttggcaaagctgcccgagatattttcaacaaaggatttggctttggactggtgaagctg
gatgtgaaaacaaagtcatgcagtggtgtggaattctcaacatctggttcatctaataca
gacactggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagaaaaatggaacaccgataatactctgggaacagaaattgcaattgaagac
cagatttgtcaaggtttgaaactgacatttgatactacattttcaccaaacacaggaaag
aaaagtggtaaaatcaagtcctcttacaagagggaatgtataaaccttggctgtgatgtt
gactttgattttgctggacctgcaatccatggttcagctgtctttggttacgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgacaaggagtaacttt
gcagtgggctacaggactggagacttccagttacatactaatgtcaataatgggacagaa
tttggaggatcaatttatcagaaagtatgtgaaaatttcgacacttcagtaaaccttgct
tggacatcaggtaccaactgcactcgttttggcattgcagctaaataccagttggatcct
actgcttccatctctgcaaaggtcaacaactctagtttaattggagtgggttacacccag
actctgaggcctggtgtgaagcttacactgtctgctctggtagatgggaagagctttaat
gctggaggccacaagcttgggcttgccttggaattggaggcttaa
DBGET
integrated database retrieval system