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Allele : Wfs1<tm1.1Bedel> wolframin ER transmembrane glycoprotein; targeted mutation 1.1, Benjamin Delprat

Primary Identifier  MGI:7571399 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Wfs1
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
molecularNote  Glutamic acid codon 864 (GAA) in exon 8 was changed to lysine (AAA) (c.2590G>A, p.E864K) and a loxP site flanked neomycin resistance gene cassette was inserted into intron 8. The neo cassette was removed through subsequent Cre-mediated recombination. The mutation is the equivalent of the same human mutation associated with Wolfram syndrome (WS).
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Wfs1<E864K>,
  • Wfs1<E864K>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories