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Allele : Del(7Herc2-Mkrn3)13FRdni deletion, Chr 7, R D Nicholls13F; deletion, Chr 7, R D Nicholls 13F
Primary Identifier  MGI:3769770 Allele Type  Transgenic
Gene  Del(7Herc2-Mkrn3)13FRdni Strain of Origin  C57BL/6 x SJL
Is Recombinase  false Is Wild Type  false
description  This deletion was generated in mice carrying Tg(Igh-Lmp2a)13FRdni. 9 lines were created with the eight others exhibiting lymphocyte cell lineage defects. Line 13F results in a deletion in chromosome 7 from Mkrn3 to Herc2 (Mkrn3, Ndn, Snurf/Snrpn, Ube3a, and Herc2 are deleted).
molecularNote  Transgene insertion of Tg(Igh-Lmp2a)13FRdni (MGI:3769767) resulted in a 5Mb deletion covering the entire Prader-Willi syndrom homology region.
  • mutations:
  • Intergenic deletion,
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Del13FRdni,
  • Tg<PWS/AS(del)>,
  • Del13FRdni,
  • Tg<PWS/AS(del)>
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1 Feature

Genome

0 Expresses

283 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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9 Publication categories





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