Equus asinus (ass): 106834658
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Entry
106834658 CDS
T04645
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
eai
Equus asinus (ass)
Pathway
eai04020
Calcium signaling pathway
eai04022
cGMP-PKG signaling pathway
eai04217
Necroptosis
eai04218
Cellular senescence
eai04613
Neutrophil extracellular trap formation
eai04621
NOD-like receptor signaling pathway
eai04979
Cholesterol metabolism
eai05010
Alzheimer disease
eai05012
Parkinson disease
eai05014
Amyotrophic lateral sclerosis
eai05016
Huntington disease
eai05017
Spinocerebellar ataxia
eai05020
Prion disease
eai05022
Pathways of neurodegeneration - multiple diseases
eai05164
Influenza A
eai05166
Human T-cell leukemia virus 1 infection
eai05208
Chemical carcinogenesis - reactive oxygen species
eai05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
eai00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
106834658 (VDAC1)
04022 cGMP-PKG signaling pathway
106834658 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
106834658 (VDAC1)
04218 Cellular senescence
106834658 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
106834658 (VDAC1)
04621 NOD-like receptor signaling pathway
106834658 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
106834658 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
106834658 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
106834658 (VDAC1)
05164 Influenza A
106834658 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
106834658 (VDAC1)
05012 Parkinson disease
106834658 (VDAC1)
05014 Amyotrophic lateral sclerosis
106834658 (VDAC1)
05016 Huntington disease
106834658 (VDAC1)
05017 Spinocerebellar ataxia
106834658 (VDAC1)
05020 Prion disease
106834658 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
106834658 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
106834658 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
eai03029
]
106834658 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
eai04040
]
106834658 (VDAC1)
Mitochondrial biogenesis [BR:
eai03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
106834658 (VDAC1)
Ion channels [BR:
eai04040
]
Chloride channels
Maxi chloride channel (VDAC)
106834658 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
106834658
NCBI-ProteinID:
XP_044636389
LinkDB
All DBs
Position
12:complement(12518349..12545112)
Genome browser
AA seq
283 aa
AA seq
DB search
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgcctcccacctacgctgatcttggcaaatccgccagggacgtcttcaccaag
ggctatggatttggcttaataaaacttgatttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctagaaacc
aagtacagatggaccgaatatggtctgacgtttacagagaaatggaacaccgacaacaca
ctaggcacggagattactgtggaagaccagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacactgggaaaaaaaatgctaagatcaagacagggtacaaacga
gagcacatcaacctgggctgcgacgtggacttcgacatcgcagggccttcaatccggggc
gccctggtgctgggttatgagggttggctggctggctaccagatgaattttgagaccgcg
aagtctcgagtgacccagagcaactttgcggttggctacaagactgatgaattccagctt
cacactaatgtaaacgatgggacagagtttggcggctccatttatcagaaggtgaacaag
aagttggagactgctgttaatctcgcctggacagcaggaaacagtaacactcgcttcgga
atagcagccaagtatcagatcgaccctgacgcgtgcttctcggctaaggtgaacaactcc
agtctgataggtttaggatacacccagaccctaaagccaggtatcaaactgacgctgtca
gctctgctggatggcaagaatgtcaacgctggtggccacaagcttggtctaggactggaa
tttcaagcataa
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