Canis lupus dingo (dingo): 118350204
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Entry
118350204 CDS
T08371
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
clud
Canis lupus dingo (dingo)
Pathway
clud04020
Calcium signaling pathway
clud04022
cGMP-PKG signaling pathway
clud04217
Necroptosis
clud04218
Cellular senescence
clud04613
Neutrophil extracellular trap formation
clud04621
NOD-like receptor signaling pathway
clud04979
Cholesterol metabolism
clud05010
Alzheimer disease
clud05012
Parkinson disease
clud05014
Amyotrophic lateral sclerosis
clud05016
Huntington disease
clud05017
Spinocerebellar ataxia
clud05020
Prion disease
clud05022
Pathways of neurodegeneration - multiple diseases
clud05164
Influenza A
clud05166
Human T-cell leukemia virus 1 infection
clud05208
Chemical carcinogenesis - reactive oxygen species
clud05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
clud00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
118350204 (VDAC1)
04022 cGMP-PKG signaling pathway
118350204 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
118350204 (VDAC1)
04218 Cellular senescence
118350204 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
118350204 (VDAC1)
04621 NOD-like receptor signaling pathway
118350204 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
118350204 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
118350204 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
118350204 (VDAC1)
05164 Influenza A
118350204 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
118350204 (VDAC1)
05012 Parkinson disease
118350204 (VDAC1)
05014 Amyotrophic lateral sclerosis
118350204 (VDAC1)
05016 Huntington disease
118350204 (VDAC1)
05017 Spinocerebellar ataxia
118350204 (VDAC1)
05020 Prion disease
118350204 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
118350204 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
118350204 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
clud03029
]
118350204 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
clud04040
]
118350204 (VDAC1)
Mitochondrial biogenesis [BR:
clud03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
118350204 (VDAC1)
Ion channels [BR:
clud04040
]
Chloride channels
Maxi chloride channel (VDAC)
118350204 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
118350204
NCBI-ProteinID:
XP_035552728
LinkDB
All DBs
Position
11:complement(21524026..21550993)
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
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggacgtcttcactaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagttcgggttcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgaatatggtctgacgtttacagagaaatggaacactgacaacact
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgctaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgtgacgtggattttgacattgctggtccttccatccggggt
gctttggtgctgggctatgagggctggctggctggctaccagatgaattttgagactgca
aagtcccgagtgacccagagcaactttgcagttggctacaagaccgacgaattccagctc
catactaacgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgtcaatctggcctggacagcaggaaatagtaacactcgctttgga
atagcggccaagtatcagattgaccccgatgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatcg
gctctgctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggag
tttcaggcgtaa
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