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Allele : Krd kidney and retinal defects
Primary Identifier  MGI:1861657 Allele Type  Transgenic
Gene  Krd Inheritance Mode  Semidominant
Strain of Origin  Not Specified Is Recombinase  false
Is Wild Type  false
molecularNote  The phenotype of this mouse has been attributed to a 7 cM transgene induced deletion, Del(19)TgN8052Mm, which includes the Pax2 and Pkd2l1. The transgene inserted into a LINE element in the distal region of Chromosome 19. The Scd1 and pale ear Hps1 genes are also deleted in Del(19)TgN8052Mm mice, along with several D19Mit markers.
  • mutations:
  • Insertion,
  • Intergenic deletion
  • synonyms:
  • Tg8052,
  • Tg8052
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1 Feature

Trail: Allele

Genome

0 Expresses

4 Mutation Involves

Trail: Allele

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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2 Carried By

Trail: Allele

0 Driven By

9 Publication categories

Trail: Allele




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