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Allele : Tg(Notch3*R169C)88Bbb transgene insertion 88, Norbert Hubner

Primary Identifier  MGI:4429538 Allele Type  Transgenic
Attribute String  Inserted expressed sequence Gene  Tg(Notch3*R169C)88Bbb
Strain of Origin  FVB/N Is Recombinase  false
Is Wild Type  false
description  Phenotypic Similarity to Human Syndrome: Cerebral Ischemic Small Vessel Disease (J:156682)
molecularNote  The transgene contains a modified rat BAC RPCI31.78K09 with the rat Notch3 gene carrying the CADASIL-associated mutation R169C. Two lines were created (88 and 92). Line 88 exhibit a 4-fold increase in expression and was selected as the representative line.
  • mutations:
  • Insertion
  • synonyms:
  • TgNotch3<R169C>,
  • TgNotch3<R169C>
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1 Feature

Trail: Allele

Genome

1 Expresses

Trail: Allele

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

13 Publication categories

Trail: Allele