Ursus americanus (American black bear): 123780315
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Entry
123780315 CDS
T07931
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
KO
K15041
voltage-dependent anion channel protein 3
Organism
uar
Ursus americanus (American black bear)
Pathway
uar04020
Calcium signaling pathway
uar04022
cGMP-PKG signaling pathway
uar04216
Ferroptosis
uar04217
Necroptosis
uar04218
Cellular senescence
uar04613
Neutrophil extracellular trap formation
uar04621
NOD-like receptor signaling pathway
uar04979
Cholesterol metabolism
uar05010
Alzheimer disease
uar05012
Parkinson disease
uar05016
Huntington disease
uar05017
Spinocerebellar ataxia
uar05020
Prion disease
uar05022
Pathways of neurodegeneration - multiple diseases
uar05161
Hepatitis B
uar05166
Human T-cell leukemia virus 1 infection
uar05203
Viral carcinogenesis
uar05208
Chemical carcinogenesis - reactive oxygen species
uar05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
uar00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
123780315 (VDAC3)
04022 cGMP-PKG signaling pathway
123780315 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
123780315 (VDAC3)
04217 Necroptosis
123780315 (VDAC3)
04218 Cellular senescence
123780315 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
123780315 (VDAC3)
04621 NOD-like receptor signaling pathway
123780315 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
123780315 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
123780315 (VDAC3)
05203 Viral carcinogenesis
123780315 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
123780315 (VDAC3)
05161 Hepatitis B
123780315 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
123780315 (VDAC3)
05012 Parkinson disease
123780315 (VDAC3)
05016 Huntington disease
123780315 (VDAC3)
05017 Spinocerebellar ataxia
123780315 (VDAC3)
05020 Prion disease
123780315 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
123780315 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
123780315 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
uar03029
]
123780315 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
uar04040
]
123780315 (VDAC3)
Mitochondrial biogenesis [BR:
uar03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
123780315 (VDAC3)
Ion channels [BR:
uar04040
]
Chloride channels
Maxi chloride channel (VDAC)
123780315 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
123780315
NCBI-ProteinID:
XP_045635111
LinkDB
All DBs
Position
Unknown
AA seq
284 aa
AA seq
DB search
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RDCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq
855 nt
NT seq
+upstream
nt +downstream
nt
atgtgtaacacaccgacttactgtgacctaggaaaggccgccaaggatgtcttcaataaa
ggatatggatttggcatggtcaagatagatctgaaaaccaagtcatgtagtggagtgatg
gaattttctacttctggtcatgcttacactgatacagggaaagcgtcaggaaacctagag
accaaatataaggtctgtaactatggacttaccttcacccagaagtggaacacagacaat
actcttggaacagaaatctctttggagaataagttggctgaaggattgaaactgactctt
gataccatatttgtaccgaacacaggaaagaagagtggaaaattgaaggcctcttacaaa
cgggattgtttcagtcttggcagtaatgttgatatagatttttctggaccaaccatctat
ggctgggctgtgttagcctttgaaggttggcttgctggctatcagatgagttttgacaca
gccaaatccaaactgtcacagaataatttcgccctgggttacaaggctgcagacttccag
ctgcacactcacgtgaatgatggcactgaatttggcgggtctatctaccagaaggttaac
gagaagattgaaacgtcgataaaccttgcttggacggctggcagtaacaatacccgtttc
ggcatcgctgctaagtacaagctggactgtaggacttctctgtctgctaaagtaaataat
gccagcctgattggactgggttatactcagacccttcgaccaggtgtcaaactgacccta
tcagctttaattgacggaaagaacttcaatgcaggaggtcacaaggttggattgggattt
gaactagaagcttaa
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