Phascolarctos cinereus (koala): 110196425
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Entry
110196425 CDS
T05867
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
KO
K15041
voltage-dependent anion channel protein 3
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04020
Calcium signaling pathway
pcw04022
cGMP-PKG signaling pathway
pcw04216
Ferroptosis
pcw04217
Necroptosis
pcw04218
Cellular senescence
pcw04613
Neutrophil extracellular trap formation
pcw04621
NOD-like receptor signaling pathway
pcw04979
Cholesterol metabolism
pcw05010
Alzheimer disease
pcw05012
Parkinson disease
pcw05016
Huntington disease
pcw05017
Spinocerebellar ataxia
pcw05020
Prion disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05161
Hepatitis B
pcw05166
Human T-cell leukemia virus 1 infection
pcw05203
Viral carcinogenesis
pcw05208
Chemical carcinogenesis - reactive oxygen species
pcw05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
110196425 (VDAC3)
04022 cGMP-PKG signaling pathway
110196425 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
110196425 (VDAC3)
04217 Necroptosis
110196425 (VDAC3)
04218 Cellular senescence
110196425 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
110196425 (VDAC3)
04621 NOD-like receptor signaling pathway
110196425 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
110196425 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
110196425 (VDAC3)
05203 Viral carcinogenesis
110196425 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
110196425 (VDAC3)
05161 Hepatitis B
110196425 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
110196425 (VDAC3)
05012 Parkinson disease
110196425 (VDAC3)
05016 Huntington disease
110196425 (VDAC3)
05017 Spinocerebellar ataxia
110196425 (VDAC3)
05020 Prion disease
110196425 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
110196425 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
110196425 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
pcw03029
]
110196425 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
pcw04040
]
110196425 (VDAC3)
Mitochondrial biogenesis [BR:
pcw03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
110196425 (VDAC3)
Ion channels [BR:
pcw04040
]
Chloride channels
Maxi chloride channel (VDAC)
110196425 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
110196425
NCBI-ProteinID:
XP_020825307
UniProt:
A0A6P5ITA4
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MCETPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHSYTDTGKASGNLET
KYKICDYGLTFVQKWNTDNTLGTEISMEDKLAEGLKVTLDTIFVPNTGKKSGKLKASYKR
DCFSLGGNVDIDFSGPTIYGWAVLAYEGWLAGYQMSFDTAKSKLSQNNFALGYKAVDFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDQKTSLSGKVNNA
SLIGLGYTQTLRAGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atgtgtgagacgccaacttactgtgacctaggaaaggctgccaaagatgtcttcaacaaa
ggatatgggtttggtatggttaaaatagatcttagaactaagtcttgcagtggagtggaa
ttttctacatctggtcattcatacactgacacaggtaaagcttcgggtaatttggaaacg
aagtacaagatctgtgactatgggcttaccttcgttcaaaaatggaacacagacaatacc
ctggggacagaaatcagcatggaggataaattggctgaaggtttgaaggtgactcttgac
accatatttgtaccaaacacaggaaagaagagtgggaaattaaaggcctcctataagcgg
gactgtttcagtcttggtggaaatgttgacattgatttctctggacccaccatctatggc
tgggccgtattggcttatgaaggttggcttgctggctatcagatgagttttgacacggcc
aaatccaaactgtctcagaataattttgccctgggttataaggctgttgacttccagctc
cacacacatgtgaatgatggcactgaatttggagggtcgatttaccaaaaggttaatgag
aagattgaaacgtcaataaatcttgcctggacagctggcagtaacaacactcgttttggc
attgctgctaagtacaagctggatcaaaaaacttctctatctggtaaagtgaataatgcc
agccttattggacttggatatactcagacactccgagcaggtgtaaaattgacactttca
gctttaattgatggaaaaaacttcaatgcaggaggtcacaaggttgggttgggatttgaa
ttggaagcttaa
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