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Allele : Gfap<tm3Mes> glial fibrillary acidic protein; targeted mutation 3, Albee Messing

Primary Identifier  MGI:3690430 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Gfap
Transmission  Germline Strain of Origin  129S7/SvEvBrd-Hprt1<+>
Is Recombinase  false Is Wild Type  false
molecularNote  The targeting vector was designed (by site-directed mutagenesis) to insert the arginine to histidine amino acid substitution at position 76 (R76H) (human 79) into exon 1 and place a loxP-flanked neomycin cassette into intron 3. R79H is associated with Alexander disease in humans. Cre-mediated recombination removed the floxed neo cassette. Quantitative real-time PCR showed that Gfap expression is elevated.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Gfap<tm1Hgmn>,
  • Gfap<tm1Hgmn>,
  • GFAP R76H,
  • GFAP R76H
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

6 Publication categories

Trail: Allele