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Allele : Adgrv1<m1> adhesion G protein-coupled receptor V1; mutation 1
Primary Identifier  MGI:6508388 Allele Type  Spontaneous
Attribute String  Null/knockout Gene  Adgrv1
Inheritance Mode  Recessive Strain of Origin  KM/Zzng
Is Recombinase  false Is Wild Type  false
molecularNote  This spontaneous single nucleotide deletion (c.6748Gdel) in exon 31, found in the Kunming strain, causes a frameshift and premature stop codon (TAA) in place of valine codon 2250 (p.V2250*fs*1).
  • mutations:
  • Intragenic deletion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

4 Publication categories





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