Carlito syrichta (Philippine tarsier): 103257263
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Entry
103257263 CDS
T07836
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
KO
K15041
voltage-dependent anion channel protein 3
Organism
csyr
Carlito syrichta (Philippine tarsier)
Pathway
csyr04020
Calcium signaling pathway
csyr04022
cGMP-PKG signaling pathway
csyr04216
Ferroptosis
csyr04217
Necroptosis
csyr04218
Cellular senescence
csyr04613
Neutrophil extracellular trap formation
csyr04621
NOD-like receptor signaling pathway
csyr04979
Cholesterol metabolism
csyr05010
Alzheimer disease
csyr05012
Parkinson disease
csyr05016
Huntington disease
csyr05017
Spinocerebellar ataxia
csyr05020
Prion disease
csyr05022
Pathways of neurodegeneration - multiple diseases
csyr05161
Hepatitis B
csyr05166
Human T-cell leukemia virus 1 infection
csyr05203
Viral carcinogenesis
csyr05208
Chemical carcinogenesis - reactive oxygen species
csyr05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
csyr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
103257263 (VDAC3)
04022 cGMP-PKG signaling pathway
103257263 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
103257263 (VDAC3)
04217 Necroptosis
103257263 (VDAC3)
04218 Cellular senescence
103257263 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
103257263 (VDAC3)
04621 NOD-like receptor signaling pathway
103257263 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
103257263 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
103257263 (VDAC3)
05203 Viral carcinogenesis
103257263 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
103257263 (VDAC3)
05161 Hepatitis B
103257263 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
103257263 (VDAC3)
05012 Parkinson disease
103257263 (VDAC3)
05016 Huntington disease
103257263 (VDAC3)
05017 Spinocerebellar ataxia
103257263 (VDAC3)
05020 Prion disease
103257263 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
103257263 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
103257263 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
csyr03029
]
103257263 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
csyr04040
]
103257263 (VDAC3)
Mitochondrial biogenesis [BR:
csyr03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
103257263 (VDAC3)
Ion channels [BR:
csyr04040
]
Chloride channels
Maxi chloride channel (VDAC)
103257263 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
103257263
NCBI-ProteinID:
XP_008053186
Ensembl:
ENSTSYG00000007112
UniProt:
A0A1U7THH3
LinkDB
All DBs
Position
Unknown
AA seq
284 aa
AA seq
DB search
MCNTPSYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RDCFSLGSNVDIDFSGPTIYGWAVLALEGWLAGYQMSFDTAKSKLSQSNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq
855 nt
NT seq
+upstream
nt +downstream
nt
atgtgtaacacgccaagttattgtgacctgggaaaggctgccaaggatgtcttcaacaaa
ggatatgggtttggcatggttaagatagatctgaaaaccaagtcttgtagtggagtgatg
gaattttctacttctggtcatgcttacactgatacagggaaagcatcaggcaacctagag
accaaatataaggtctgcaactatggacttaccttcacccaaaaatggaacacagacaat
actcttgggacagagatctctttggagaataagttggctgaagggttgaaactgactctc
gataccatatttgtaccaaacacaggaaagaagagtgggaaattgaaggcctcttataaa
cgggattgtttcagtcttggcagtaatgttgatatagatttttctgggccaaccatctat
ggctgggctgtgttggccttagaagggtggcttgctggctatcagatgagttttgataca
gccaaatccaaactgtcacagagtaatttcgccctgggttacaaggctgcagacttccag
ctgcacactcatgtgaatgatggcactgaatttggaggttctatctaccagaaggttaat
gagaagattgaaacgtcaataaaccttgcttggacagctggcagtaacaacacccgtttt
ggcattgctgctaaatacaagttggattgtagaacttctctatctgctaaagtaaataat
gccagcctgattggactgggttatactcagacccttcgaccaggagtcaaactgaccttg
tcagctttaattgatggaaagaacttcaatgcaggaggtcacaaggttgggttgggtttt
gaactggaagcttaa
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