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Allele : Hnf1b<tm2.1Sce> HNF1 homeobox B; targeted mutation 2.1, Silvia Cereghini

Primary Identifier  MGI:6715604 Allele Type  Targeted
Attribute String  Hypomorph Gene  Hnf1b
Transmission  Germline Strain of Origin  129
Is Recombinase  false Is Wild Type  false
molecularNote  A G to T change was made at the intron 2 splice donor site (GAC/g taagtgttttaacctt to GAC/t taagtgttttaagctt) reproducing the c.544+1G>T human spicing point mutation. In addition, a loxP-flanked neomycin resistance cassette was inserted within intron 1 and excised via cre-mediated recombination. Transcript and protein levels are reduced during development and levels of protein, but not transcript, are reduced in postnatal life in heterozygotes. None of the potential truncated proteins encoded by alternative spliced transcripts are detected.
  • mutations:
  • Single point mutation
  • synonyms:
  • Hnf1b<Sp2>,
  • Hnf1b<Sp2>
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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

3 Publication categories

Trail: Allele