Mustela lutreola (European mink): 131832037
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Entry
131832037 CDS
T09578
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
mlk
Mustela lutreola (European mink)
Pathway
mlk04020
Calcium signaling pathway
mlk04022
cGMP-PKG signaling pathway
mlk04217
Necroptosis
mlk04218
Cellular senescence
mlk04613
Neutrophil extracellular trap formation
mlk04621
NOD-like receptor signaling pathway
mlk04979
Cholesterol metabolism
mlk05010
Alzheimer disease
mlk05012
Parkinson disease
mlk05014
Amyotrophic lateral sclerosis
mlk05016
Huntington disease
mlk05017
Spinocerebellar ataxia
mlk05020
Prion disease
mlk05022
Pathways of neurodegeneration - multiple diseases
mlk05164
Influenza A
mlk05166
Human T-cell leukemia virus 1 infection
mlk05208
Chemical carcinogenesis - reactive oxygen species
mlk05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
mlk00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
131832037 (VDAC1)
04022 cGMP-PKG signaling pathway
131832037 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
131832037 (VDAC1)
04218 Cellular senescence
131832037 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
131832037 (VDAC1)
04621 NOD-like receptor signaling pathway
131832037 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
131832037 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
131832037 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
131832037 (VDAC1)
05164 Influenza A
131832037 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
131832037 (VDAC1)
05012 Parkinson disease
131832037 (VDAC1)
05014 Amyotrophic lateral sclerosis
131832037 (VDAC1)
05016 Huntington disease
131832037 (VDAC1)
05017 Spinocerebellar ataxia
131832037 (VDAC1)
05020 Prion disease
131832037 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
131832037 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
131832037 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mlk03029
]
131832037 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
mlk04040
]
131832037 (VDAC1)
Mitochondrial biogenesis [BR:
mlk03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
131832037 (VDAC1)
Ion channels [BR:
mlk04040
]
Chloride channels
Maxi chloride channel (VDAC)
131832037 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
131832037
NCBI-ProteinID:
XP_059030557
LinkDB
All DBs
Position
5:complement(72538833..72574628)
Genome browser
AA seq
283 aa
AA seq
DB search
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGAVVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggccgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacaggtggaccgaatatggtctgacgtttacagagaaatggaacactgacaacacg
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgcaaaaatcaagacagggtataagcgg
gagcacatcaacctaggctgcgatgtggatttcgacattgccggtccttcagtccggggt
gccgtggtgctgggctatgaaggctggctggctggctaccagatgaattttgagactgcg
aagtctcgagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctc
cacactaatgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagactgctgtcaatctggcctggactgcaggaaatagtaacactcgctttgga
atagcagccaaatatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatca
gctctgctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa
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