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Center for Computational Systems Medicine
Soverview

Gene summary

Soverview

RNA A-to-I events

Soverview

Differntial gene expression between RNA A-to-I edited tumor samples versus normal samples

Soverview

Protein coding region RNA A-to-I editings

Soverview

The effects of the RNA editing to the miRNA binding sites

Soverview

The effects of the RNA editing to the stability of the RNA structures

Soverview

Relation with ADAR

Soverview

Relation with cancer stages

Soverview

Relation with survival state

Soverview

Related drugs with this gene

Soverview

Related diseases with this gene

Editing gene: SLC18A2 (CAeditome ID:6571)

Gene summary for SLC18A2

check button Gene summary
Gene informationGene symbol

SLC18A2

Gene ID

6571

Gene namesolute carrier family 18 member A2
SynonymsPKDYS2|SVAT|SVMT|VAT2|VMAT2
Cytomap

10q25.3

Type of geneprotein-coding
Descriptionsynaptic vesicular amine transportermonoamine neurotransmitter transportersolute carrier family 18 (vesicular monoamine transporter), member 2synaptic vesicle amine transporter, brainsynaptic vesicle monoamine transporter, brainvesicle monoamine tran
Modification date20210518
UniProtAcc

Q05940

Context

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID
SLC18A2

GO:0005813

Synaptic vesicular amine transporter

0000052

SLC18A2

GO:0043231

Synaptic vesicular amine transporter

0000052


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RNA A-to-I events for SLC18A2

check buttonRNA A-to-I editing events across TCGA 33 cancers data sets based on Ensembl gene isoform structure.
all structure

check button RNA editing frequencies across 33 cancers of gene: ENSG00000165646.10

check button RNA A-to-I editing events in Cancer.
CAediting_784692(117258884, +), CAediting_784693(117258896, +), CAediting_784694(117261102, +), CAediting_784695(117261103, +), CAediting_784696(117261108, +), CAediting_784697(117261111, +), CAediting_784698(117261162, +), CAediting_784699(117261165, +), CAediting_784700(117261171, +), CAediting_784701(117261251, +), CAediting_784702(117261261, +), CAediting_784703(117261264, +), CAediting_784704(117261271, +), CAediting_784705(117261276, +), CAediting_784706(117261277, +), CAediting_784707(117261287, +), CAediting_784708(117261310, +), CAediting_784709(117261313, +), CAediting_784710(117262007, +), CAediting_784711(117262008, +), CAediting_784712(117262047, +), CAediting_784713(117262087, +), CAediting_784714(117262104, +), CAediting_784715(117262107, +), CAediting_784716(117262121, +), CAediting_784717(117262157, +), CAediting_784718(117262179, +), CAediting_784719(117262734, +), CAediting_784720(117262744, +), CAediting_784721(117262755, +), CAediting_784722(117262756, +), CAediting_784723(117262769, +), CAediting_784724(117262770, +), CAediting_784725(117262787, +), CAediting_784726(117262797, +), CAediting_784727(117262800, +), CAediting_784728(117264355, +), CAediting_784729(117264356, +), CAediting_784730(117264391, +), CAediting_784731(117264402, +), CAediting_784732(117264420, +), CAediting_784733(117264421, +), CAediting_784734(117264426, +), CAediting_784735(117265835, +), CAediting_784736(117265914, +), CAediting_784737(117265975, +), CAediting_784738(117265979, +), CAediting_784739(117265996, +), CAediting_784740(117265997, +), CAediting_784741(117266005, +), CAediting_784742(117266011, +), CAediting_784743(117266039, +), CAediting_784744(117266040, +), CAediting_784745(117268816, +), CAediting_784746(117268820, +), CAediting_784747(117268936, +), CAediting_784748(117268956, +), CAediting_784749(117268960, +), CAediting_784750(117268964, +),

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RNA editing positional annotations for SLC18A2 using Annovar

check button Protein coding RNA editing(s).
CAeditome IDPositionVariant typeENSTNTchangeAAchangeSIFT_scorePolyphen2_HVAR_scorePROVEAN_pred

check button Gene structure information of RNA editing(s).
CAeditome IDPositionVariant type
CAediting_784692chr10_117258884_+ncRNA_intronic
CAediting_784693chr10_117258896_+ncRNA_intronic
CAediting_784694chr10_117261102_+ncRNA_intronic
CAediting_784695chr10_117261103_+ncRNA_intronic
CAediting_784696chr10_117261108_+ncRNA_intronic
CAediting_784697chr10_117261111_+ncRNA_intronic
CAediting_784698chr10_117261162_+ncRNA_intronic
CAediting_784699chr10_117261165_+ncRNA_intronic
CAediting_784700chr10_117261171_+ncRNA_intronic
CAediting_784701chr10_117261251_+ncRNA_intronic
CAediting_784702chr10_117261261_+ncRNA_intronic
CAediting_784703chr10_117261264_+ncRNA_intronic
CAediting_784704chr10_117261271_+ncRNA_intronic
CAediting_784705chr10_117261276_+ncRNA_intronic
CAediting_784706chr10_117261277_+ncRNA_intronic
CAediting_784707chr10_117261287_+ncRNA_intronic
CAediting_784708chr10_117261310_+ncRNA_intronic
CAediting_784709chr10_117261313_+ncRNA_intronic
CAediting_784710chr10_117262007_+ncRNA_intronic
CAediting_784711chr10_117262008_+ncRNA_intronic
CAediting_784712chr10_117262047_+ncRNA_intronic
CAediting_784713chr10_117262087_+ncRNA_intronic
CAediting_784714chr10_117262104_+ncRNA_intronic
CAediting_784715chr10_117262107_+ncRNA_intronic
CAediting_784716chr10_117262121_+ncRNA_intronic
CAediting_784717chr10_117262157_+ncRNA_intronic
CAediting_784718chr10_117262179_+ncRNA_intronic
CAediting_784719chr10_117262734_+ncRNA_intronic
CAediting_784720chr10_117262744_+ncRNA_intronic
CAediting_784721chr10_117262755_+ncRNA_intronic
CAediting_784722chr10_117262756_+ncRNA_intronic
CAediting_784723chr10_117262769_+ncRNA_intronic
CAediting_784724chr10_117262770_+ncRNA_intronic
CAediting_784725chr10_117262787_+ncRNA_intronic
CAediting_784726chr10_117262797_+ncRNA_intronic
CAediting_784727chr10_117262800_+ncRNA_intronic
CAediting_784728chr10_117264355_+ncRNA_intronic
CAediting_784729chr10_117264356_+ncRNA_intronic
CAediting_784730chr10_117264391_+ncRNA_intronic
CAediting_784731chr10_117264402_+ncRNA_intronic
CAediting_784732chr10_117264420_+ncRNA_intronic
CAediting_784733chr10_117264421_+ncRNA_intronic
CAediting_784734chr10_117264426_+ncRNA_intronic
CAediting_784735chr10_117265835_+ncRNA_intronic
CAediting_784736chr10_117265914_+ncRNA_intronic
CAediting_784737chr10_117265975_+ncRNA_intronic
CAediting_784738chr10_117265979_+ncRNA_intronic
CAediting_784739chr10_117265996_+ncRNA_intronic
CAediting_784740chr10_117265997_+ncRNA_intronic
CAediting_784741chr10_117266005_+ncRNA_intronic
CAediting_784742chr10_117266011_+ncRNA_intronic
CAediting_784743chr10_117266039_+ncRNA_intronic
CAediting_784744chr10_117266040_+ncRNA_intronic
CAediting_784745chr10_117268816_+ncRNA_intronic
CAediting_784746chr10_117268820_+ncRNA_intronic
CAediting_784747chr10_117268936_+ncRNA_intronic
CAediting_784748chr10_117268956_+ncRNA_intronic
CAediting_784749chr10_117268960_+ncRNA_intronic
CAediting_784750chr10_117268964_+ncRNA_intronic

check button Repat-regional RNA editing(s).
CAeditome IDPositionRepeat familyRepeat sub familyRepeat name
CAediting_784692chr10_117258884_+SINEAluAluSx
CAediting_784693chr10_117258896_+SINEAluAluSx
CAediting_784694chr10_117261102_+SINEAluAluJr
CAediting_784695chr10_117261103_+SINEAluAluJr
CAediting_784696chr10_117261108_+SINEAluAluJr
CAediting_784697chr10_117261111_+SINEAluAluJr
CAediting_784698chr10_117261162_+SINEAluAluJr
CAediting_784699chr10_117261165_+SINEAluAluJr
CAediting_784700chr10_117261171_+SINEAluAluJr
CAediting_784701chr10_117261251_+SINEAluAluJr
CAediting_784702chr10_117261261_+SINEAluAluJr
CAediting_784703chr10_117261264_+SINEAluAluJr
CAediting_784704chr10_117261271_+SINEAluAluJr
CAediting_784705chr10_117261276_+SINEAluAluJr
CAediting_784706chr10_117261277_+SINEAluAluJr
CAediting_784707chr10_117261287_+SINEAluAluJr
CAediting_784708chr10_117261310_+SINEAluAluJr
CAediting_784709chr10_117261313_+SINEAluAluJr
CAediting_784710chr10_117262007_+SINEAluAluSg4
CAediting_784711chr10_117262008_+SINEAluAluSg4
CAediting_784712chr10_117262047_+SINEAluAluSg4
CAediting_784713chr10_117262087_+SINEAluAluSg4
CAediting_784714chr10_117262104_+SINEAluAluSg4
CAediting_784715chr10_117262107_+SINEAluAluSg4
CAediting_784716chr10_117262121_+SINEAluAluSg4
CAediting_784717chr10_117262157_+SINEAluAluSg4
CAediting_784718chr10_117262179_+SINEAluAluSg4
CAediting_784719chr10_117262734_+SINEAluAluJb
CAediting_784720chr10_117262744_+SINEAluAluJb
CAediting_784721chr10_117262755_+SINEAluAluJb
CAediting_784722chr10_117262756_+SINEAluAluJb
CAediting_784723chr10_117262769_+SINEAluAluJb
CAediting_784724chr10_117262770_+SINEAluAluJb
CAediting_784725chr10_117262787_+SINEAluAluJb
CAediting_784726chr10_117262797_+SINEAluAluJb
CAediting_784727chr10_117262800_+SINEAluAluJb
CAediting_784728chr10_117264355_+SINEAluAluSx
CAediting_784729chr10_117264356_+SINEAluAluSx
CAediting_784730chr10_117264391_+SINEAluAluSx
CAediting_784731chr10_117264402_+SINEAluAluSx
CAediting_784732chr10_117264420_+SINEAluAluSx
CAediting_784733chr10_117264421_+SINEAluAluSx
CAediting_784734chr10_117264426_+SINEAluAluSx
CAediting_784735chr10_117265835_+SINEAluAluSx
CAediting_784736chr10_117265914_+SINEAluAluSx
CAediting_784737chr10_117265975_+SINEAluAluSx
CAediting_784738chr10_117265979_+SINEAluAluSx
CAediting_784739chr10_117265996_+SINEAluAluSx
CAediting_784740chr10_117265997_+SINEAluAluSx
CAediting_784741chr10_117266005_+SINEAluAluSx
CAediting_784742chr10_117266011_+SINEAluAluSx
CAediting_784743chr10_117266039_+SINEAluAluSx
CAediting_784744chr10_117266040_+SINEAluAluSx
CAediting_784745chr10_117268816_+Simple_repeatSimple_repeat(TG)n
CAediting_784746chr10_117268820_+Simple_repeatSimple_repeat(TG)n
CAediting_784747chr10_117268936_+Simple_repeatSimple_repeat(ACACAT)n
CAediting_784748chr10_117268956_+Simple_repeatSimple_repeat(ACACAT)n
CAediting_784749chr10_117268960_+Simple_repeatSimple_repeat(ACACAT)n
CAediting_784750chr10_117268964_+Simple_repeatSimple_repeat(ACACAT)n

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RNA A-to-I editing events in the alternative splicing sites for SLC18A2

check button RNA A-to-I editing(s) in the alternative splicing sites.
AStypeCAeditomIDEditing positionAS positionAS directionExonic locationWildtype sequenceWildtype splicing strengthRNA edited sequenceRNA edited splicing strength

check button Differential percent of spliced in (PSI) between RNA A-to-I edited and non-edited samples for ENSG00000165646.10.SLC18A2.

check button Correlation between RNA A-to-I editing and PSI for ENSG00000165646.10.SLC18A2.

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Differntial gene expression between RNA A-to-I edited versus non-edited samples for SLC18A2

check button Differential gene expressions between RNA A-to-I edited and non-edited tumor samples.
* The grey color means N/A.
boxplot

check button Correlation between RNA A-to-I editing and gene expression.
boxplot

check button - Differentially expressed gene between RNA A-to-I edited samples versus non-edited samples.
* Click on the image to enlarge it in a new window.
PCPG.CAediting_784729.ENSG00000165646.SLC18A2.png
Soverview

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Protein coding region RNA A-to-I editings for SLC18A2

check button- Lollipop plot for RNA A-to-I editings across protein structure.
* Click on the image to enlarge it in a new window.


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The effects of the RNA editing to the miRNA binding sites for SLC18A2

**If you are searching a miRNA gene with RNA editing events in its seed regions, please see the search pages of miRNA targets to discover the effects of this RNA editing event to miRNA regulations. For more information, please check the files in the Download page.

check button RNA A-to-I editing in the 3'-UTR regions of mRNA gained miRNA binding sites.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in the 3'-UTR regions of mRNA lost miRNA binding sites.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in lncRNA gained miRNA binding sites.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in lncRNA lost miRNA binding sites.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in miRNAs gained binding to lncRNA.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in miRNAs lost binding to lncRNA.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in miRNAs gained binding to the 3'-UTR region of mRNA.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button RNA A-to-I editing in miRNAs lost binding to the 3'-UTR mRNA.
CAeditom_IDPositionENSGENSTmiRNATargetscan startTargetscan endTargetscan scoreMiranda startMiranda endMiranda scoreMiranda energy

check button Differentially expressed gene-miRNA network

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The effects of the RNA editing to the stability of the RNA structures for SLC18A2

check button - RNA A-to-I editing in mRNA.
* Click on the image to enlarge it in a new window.
ENSTENST typeRNA structure without RNA A-to-I editing.RNA structure with RNA A-to-I editing.

check button RNA A-to-I editing in RNA structures for Minimum free energy (MFE).
CAeditom_IDENSTEditing_PositionMFE_withoneAIMFE_withoutAIMFE_withmultipleAI

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Relation with ADAR for SLC18A2

check button Correlation between ADAR gene expression and RNA editing frequency
CancerCAeditomIDpositionADAR1 (p-val)ADAR1 (coeff.)ADAR2 (p-val)ADAR2 (coeff.)ADAR3 (p-val)ADAR3 (coeff.)

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Relation with cancer stages for SLC18A2

check button Correlation between Cancer stages and RNA editing frequency
CancerStage_typeCAeditomIDpositionP-valCoeff.

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Relation with survival for SLC18A2

check button Correlation between RNA editing and survival
CancerCAeditomIDpositionKMpvalueCoxpvalueCoxHR

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RelatedDrugs for SLC18A2

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.8 2021-01-03)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
SLC18A2Q05940DB00368NorepinephrineSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB00502HaloperidolSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB00988DopamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB01089DeserpidineSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB06706IsomethepteneSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB06714PropylhexedrineSynaptic vesicular amine transporter SmallMoleculeDrugapproved
SLC18A2Q05940DB00865BenzphetamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|illicit
SLC18A2Q05940DB01576DextroamphetamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|illicit
SLC18A2Q05940DB01577MetamfetamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|illicit
SLC18A2Q05940DB00182AmphetamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|illicit|investigational
SLC18A2Q05940DB00206ReserpineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|investigational
SLC18A2Q05940DB00579MazindolSynaptic vesicular amine transporter SmallMoleculeDrugapproved|investigational
SLC18A2Q05940DB04844TetrabenazineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|investigational
SLC18A2Q05940DB05381HistamineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|investigational
SLC18A2Q05940DB12161DeutetrabenazineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|investigational
SLC18A2Q05940DB04821NomifensineSynaptic vesicular amine transporter SmallMoleculeDrugapproved|withdrawn

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RelatedDiseases for SLC18A2

check button Diseases associated with this gene.
(DisGeNet 7.0)
GeneDisease IDDisease name# pubmedsSource
SLC18A2C0011570Mental Depression5PSYGENET
SLC18A2C0011581Depressive disorder5PSYGENET
SLC18A2C0001973Alcoholic Intoxication, Chronic3PSYGENET
SLC18A2C0005586Bipolar Disorder3PSYGENET
SLC18A2C0036341Schizophrenia3PSYGENET
SLC18A2C0027746Nerve Degeneration1CTD_human
SLC18A2C0027765nervous system disorder1CTD_human
SLC18A2C0030567Parkinson Disease1CTD_human
SLC18A2C0236701Cocaine-induced mood disorder1PSYGENET
SLC18A2C0242422Parkinsonian Disorders1CTD_human
SLC18A2C0242423Ramsay Hunt Paralysis Syndrome1CTD_human
SLC18A2C0270458Severe major depression with psychotic features1PSYGENET
SLC18A2C0600427Cocaine Dependence1PSYGENET
SLC18A2C0752097Autosomal Dominant Juvenile Parkinson Disease1CTD_human
SLC18A2C0752098Autosomal Dominant Parkinsonism1CTD_human
SLC18A2C0752100Autosomal Recessive Parkinsonism1CTD_human
SLC18A2C0752101Parkinsonism, Experimental1CTD_human
SLC18A2C0752104Familial Juvenile Parkinsonism1CTD_human
SLC18A2C0752105Parkinsonism, Juvenile1CTD_human
SLC18A2C1868675PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE1CTD_human
SLC18A2C4747991PARKINSONISM-DYSTONIA, INFANTILE, 21ORPHANET;UNIPROT