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XB-GENEPAGE-961534
???displayGene.symbol???: slc5a7
???displayGene.name???: solute carrier family 5 (sodium/choline cotransporter), member 7
???displayGene.synonyms???
cht1
(
???displayGene.geneFunction??? Choline transporter Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: Disease Ontology: autosomal dominant distal hereditary motor neuronopathy 7
MIM:
MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20
External Links:
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???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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