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Allele : Slc2a1<Rgsc200> solute carrier family 2 (facilitated glucose transporter), member 1; RIKEN Genomic Sciences Center (GSC), 200

Primary Identifier  MGI:3811855 Allele Type  Chemically induced (ENU)
Gene  Slc2a1 Inheritance Mode  Dominant
Strain of Origin  C57BL/6JJcl Is Recombinase  false
Is Wild Type  false Project Collection  RIKEN GSC ENU Project
molecularNote  This mutation was identified in an ENU mutagenesis screen. Sequence analysis of the gene revealed a T-to-C mutation in exon 7. The mutation resulted in a substitution of serine with proline at residue 324 of the encoded protein. RT-qPCR analysis showed a significant increase of Slc2a1 mRNA expression in the forebrain of adult heterozygotes. Immunoblotting showed no significant alterations of SLC2A1 protein expression in the forebrain of adult heterozygotes relative to wild-type controls.
  • mutations:
  • Single point mutation
  • synonyms:
  • Glut1<Rgsc200>,
  • Glut1<Rgsc200>,
  • M100200,
  • M100200
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

4 Publication categories