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ECB-GENEPAGE-23168598
???displayGene.symbol??? slc35a2
![]() Symbol Status
![]() ???displayGene.name??? solute carrier family 35 member A2
![]() Name Status
![]() ???displayGene.synonyms???
LOC110982879
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LOC582566
,
Solute carrier family 35 member A2
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Sp-Slc35a2
,
SPU_009014
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UDP-Gal-Tr
[+]
(
???displayGene.geneFunction??? Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: Disease Ontology: congenital disorder of glycosylation type II
MIM:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M
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)