Talpa occidentalis (Iberian mole): 119243472
Help
Entry
119243472 CDS
T07495
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
tod
Talpa occidentalis (Iberian mole)
Pathway
tod04020
Calcium signaling pathway
tod04022
cGMP-PKG signaling pathway
tod04217
Necroptosis
tod04218
Cellular senescence
tod04613
Neutrophil extracellular trap formation
tod04621
NOD-like receptor signaling pathway
tod04979
Cholesterol metabolism
tod05010
Alzheimer disease
tod05012
Parkinson disease
tod05014
Amyotrophic lateral sclerosis
tod05016
Huntington disease
tod05017
Spinocerebellar ataxia
tod05020
Prion disease
tod05022
Pathways of neurodegeneration - multiple diseases
tod05164
Influenza A
tod05166
Human T-cell leukemia virus 1 infection
tod05208
Chemical carcinogenesis - reactive oxygen species
tod05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
tod00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
119243472 (VDAC1)
04022 cGMP-PKG signaling pathway
119243472 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
119243472 (VDAC1)
04218 Cellular senescence
119243472 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
119243472 (VDAC1)
04621 NOD-like receptor signaling pathway
119243472 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
119243472 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
119243472 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
119243472 (VDAC1)
05164 Influenza A
119243472 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
119243472 (VDAC1)
05012 Parkinson disease
119243472 (VDAC1)
05014 Amyotrophic lateral sclerosis
119243472 (VDAC1)
05016 Huntington disease
119243472 (VDAC1)
05017 Spinocerebellar ataxia
119243472 (VDAC1)
05020 Prion disease
119243472 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
119243472 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
119243472 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
tod03029
]
119243472 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
tod04040
]
119243472 (VDAC1)
Mitochondrial biogenesis [BR:
tod03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
119243472 (VDAC1)
Ion channels [BR:
tod04040
]
Chloride channels
Maxi chloride channel (VDAC)
119243472 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
119243472
NCBI-ProteinID:
XP_037365227
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MAVPPTYIDLGKPARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgcctcccacgtacattgatcttggcaaacccgccagggatgtcttcaccaag
ggttatggatttggtttaatcaagcttgatttgaaaacaaagtctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgaatacggtctgacgtttacagagaaatggaacactgacaacaca
ctaggcaccgagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttttcacccaacactgggaaaaaaaatgctaaaatcaagacagggtacaagcga
gagcacatcaacctgggctgtgacgtggactttgacatcgccgggccctccatccggggc
gccctggtgctgggctatgagggctggctggctggctaccagatgaattttgagaccgcc
aagtctcgagtgacccagagcaactttgcggtgggctacaagaccgacgaattccagctt
cacactaatgtaaatgatgggacagagtttggtggctccatttaccagaaggtgaacaag
aagttggagactgccgttaatcttgcctggacagcaggcaacagcaacactcgcttcgga
atagcagccaaatatcagattgaccctgatgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacactgtca
gctctgctggatggcaagaatgtcaacgcgggtggccacaagcttggtctaggactggaa
tttcaagcataa
DBGET
integrated database retrieval system