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Allele : Grm6<nob8> glutamate receptor, metabotropic 6; no b wave 8

Primary Identifier  MGI:5754533 Allele Type  Spontaneous
Attribute String  Hypomorph Gene  Grm6
Inheritance Mode  Recessive Strain of Origin  CBA/CaJ
Is Recombinase  false Is Wild Type  false
molecularNote  This spontaneous A-to-T transversion at position Chr11:50851337 (GRCm38) results in a missense mutation at position 66, changing methionine to leucine (p.M66L). This residue lies in the glutamate binding region and is invariant across many mammals including human.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

7 Publication categories