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ECB-GENEPAGE-23037065
???displayGene.symbol??? slc18a3
![]() Symbol Status
![]() ???displayGene.name??? solute carrier family 18 member A3
![]() Name Status
![]() ???displayGene.synonyms???
LOC115917906
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probable vesicular acetylcholine transporter-B
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Sp-Vacht
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SPU_006161
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Vesicular Acetylcholine Transporter
[-]
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???displayGene.geneFunction??? Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: MIM:
MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC; CMS21
External Links:
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Symbol legend:
![](img/icons/rocket.gif)
![](img/icons/magnifying_glass.png)
![](img/icons/images.gif)
![](img/icons/info1_blue.png)