Slc2a1 (solute carrier family 2 (facilitated glucose transporter), member 1)

基因基本信息

Slc2a1 基因表型（MGI）

Homozygous null embryos are small, lack visibly detectable eyes, show a diminutive rostral embryonic pole and an overall developmental delay, and die at E10-E14. Heterozygotes show spontaneous seizures, impaired motor performance, hypoglycorrhachia, microencephaly, and reduced brain glucose uptake. Mice homozygous for the p.P485L mutation die immediately after birth.

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