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Allele : Uchl1<gad> ubiquitin carboxy-terminal hydrolase L1; gracile axonal dystrophy

Primary Identifier  MGI:1856882 Allele Type  Spontaneous
Gene  Uchl1 Inheritance Mode  Recessive
Strain of Origin  (CBA/Nga x RFM/Nga)F2 Is Recombinase  false
Is Wild Type  false
molecularNote  The mutation in the gad mouse is an in-frame deletion including exons 7 and 8. A truncated protein is encoded that is lacking a segment of 42 amino acids containing a catalytic residue.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • gad,
  • gad
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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

35 Publication categories

Trail: Allele