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Allele : Igs2<tm1Kng> intergenic site 2; targeted mutation 1, David M Kingsley

Primary Identifier  MGI:6095646 Allele Type  Targeted
Attribute String  Reporter Gene  Igs2
Transmission  Germline Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Is Recombinase  false Is Wild Type  false
description  ES cell line = FVB-H11P3, a 129-derived embryonic stem cell line (R1) carrying three tandem attP sites (P3) at Hipp11.
molecularNote  The targeting construct contains an attB site, mouse Hsp68 minimal promoter, a human regulatory region (H2), mouse Kitl cDNA, SV40, an attB site and FRT5. The construct and phiC31 mRNA were co-injected into a single pronucleus of FVB-H11P3 zygotes. H2 is regulatory enhancer located in an intergenic region 350 kb upstream of the Kitl transcription start site, it contains a non-coding SNP (rs12821256) associated with hair color. The ancestral (ANC) polymorphism (A) is associated with brown hair, and the BLD polymorphism (G) is associated with blond hair. This allele carries the A polymorphism.
  • mutations:
  • Insertion
  • synonyms:
  • ANC-Kitlg,
  • ANC-Kitlg
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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

3 Publication categories

Trail: Allele