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Allele : Htt<tm4.1Ics> huntingtin; targeted mutation 4.1, Mouse Clinical Institute

Primary Identifier  MGI:6501794 Allele Type  Targeted
Attribute String  Not Specified Gene  Htt
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
molecularNote  Mutations were engineered in exon 27 to change serine codons (TCA) 1160 and 1180 to aspartic acid codons (CTA) (p.S1160D, p.S1180D). The loxP site flanked neomycin resistance gene cassette that was inserted into intron 27 was removed through subsequent cre-mediated recombination. The substitution of the two serines with aspartic acids acts as a phosphomimic (i.e. mimics the constitutive phosphorylation of the two residues).
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Hdh<S1181D/S1201D>,
  • Hdh<S1181D/S1201D>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele