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Allele : Slc6a5<trsl> solute carrier family 6 (neurotransmitter transporter, glycine), member 5; tremor with stiff legged walk
Primary Identifier  MGI:5796925 Allele Type  Chemically induced (ENU)
Attribute String  Hypomorph Gene  Slc6a5
Inheritance Mode  Recessive Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
molecularNote  A single G-to-A point transition at chromosome 7 position 49,917,609 (GRCm38/mm10) causes the codon change of atG to atA resulting in the change of methionine to isoleucine in a transmembrane domain, p.M278I in NP_001139485.1 and p.M2701I in NP_683733.2.
  • 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

4 Publication categories





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