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Allele : Itpr1<wblo> inositol 1,4,5-trisphosphate receptor 1; wobbly locomotion

Primary Identifier  MGI:4437432 Allele Type  Spontaneous
Gene  Itpr1 Inheritance Mode  Recessive
Strain of Origin  B6;129-Gla<tm1Kul>/J Is Recombinase  false
Is Wild Type  false
molecularNote  This spontaneous mutation was identified at The Jackson Laboratory. The molecular lesion is a G-to-A mutation at coding nucleotide 1166 of the cDNA (NM_010585) which alters an arginine to a histidine at position 389 of the encoded protein (p.R389H).
  • mutations:
  • Single point mutation
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele