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XB-GENEPAGE-482084
???displayGene.symbol???: slc4a11
???displayGene.name???: solute carrier family 4 member 11
???displayGene.synonyms???
XNBC2
(
???displayGene.geneFunction??? transmembrane solute exchange Protein Function
![]() ???displayGene.geneInteractants???
Human Physical (1), Co-citation (26)
Diseases: Disease Ontology: congenital hereditary endothelial dystrophy of cornea
MIM:
CORNEAL ENDOTHELIAL DYSTROPHY; CHED
External Links:
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Gene ID & Location |
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???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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