Mustela lutreola (European mink): 131820455
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Entry
131820455 CDS
T09578
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
KO
K15041
voltage-dependent anion channel protein 3
Organism
mlk
Mustela lutreola (European mink)
Pathway
mlk04020
Calcium signaling pathway
mlk04022
cGMP-PKG signaling pathway
mlk04216
Ferroptosis
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
mlk05016
Huntington disease
mlk05017
Spinocerebellar ataxia
mlk05020
Prion disease
mlk05022
Pathways of neurodegeneration - multiple diseases
mlk05161
Hepatitis B
mlk05166
Human T-cell leukemia virus 1 infection
mlk05203
Viral carcinogenesis
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
131820455 (VDAC3)
04022 cGMP-PKG signaling pathway
131820455 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
131820455 (VDAC3)
04217 Necroptosis
131820455 (VDAC3)
04218 Cellular senescence
131820455 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
131820455 (VDAC3)
04621 NOD-like receptor signaling pathway
131820455 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
131820455 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
131820455 (VDAC3)
05203 Viral carcinogenesis
131820455 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
131820455 (VDAC3)
05161 Hepatitis B
131820455 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
131820455 (VDAC3)
05012 Parkinson disease
131820455 (VDAC3)
05016 Huntington disease
131820455 (VDAC3)
05017 Spinocerebellar ataxia
131820455 (VDAC3)
05020 Prion disease
131820455 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
131820455 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
131820455 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mlk03029
]
131820455 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
mlk04040
]
131820455 (VDAC3)
Mitochondrial biogenesis [BR:
mlk03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
131820455 (VDAC3)
Ion channels [BR:
mlk04040
]
Chloride channels
Maxi chloride channel (VDAC)
131820455 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
131820455
NCBI-ProteinID:
XP_059012052
LinkDB
All DBs
Position
18:complement(4246917..4260689)
Genome browser
AA seq
288 aa
AA seq
DB search
MFLNNMCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVEFSTSGHAYTDTGKAS
GNLETKYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLK
ASYKRDCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKA
ADFQLHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDYRTSLSA
KVNNASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq
867 nt
NT seq
+upstream
nt +downstream
nt
atgtttctaaacaatatgtgtaacacgccgacttactgtgacctaggaaaggccgcgaag
gatgtcttcaataaaggatatggatttggcatggtcaaaatagatctgaaaaccaagtcc
tgtagtggagtggaattttctacttctggtcatgcctacactgatacagggaaagcgtca
ggcaacctagagaccaaatataaggtctgtaactatggacttaccttcactcagaaatgg
aatacagacaatactcttggaacagaaatctctttggagaataagttggctgaagggttg
aaactgactcttgataccatatttgtaccgaacacaggaaagaagagtggaaaattgaag
gcctcgtataaacgggattgtttcagtcttggcagtaatgttgatattgatttttctgga
ccaaccatctatggctgggctgtgttagcttttgaaggttggcttgctggctatcagatg
agttttgacacagccaaatccaaactgtcacagaataatttcgccctgggttacaaggct
gcggacttccagctgcacactcatgtgaatgatggcactgaatttggagggtctatctac
cagaaggttaacgagaagatagaaacgtcaataaaccttgcttggacggccggcagtaac
aacacccgttttggcatcgctgctaaatacaagctggactatagaacttctctgtctgct
aaagtaaataatgccagcctgatcggactgggttatactcagacccttcgaccgggcgtc
aaactgaccctgtcagctttaatcgacggaaagaacttcaatgcaggaggtcacaaggtt
gggttgggatttgaactagaagcttaa
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