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Allele : Slc12a6<gaxp> solute carrier family 12, member 6; giant axonopathy
Primary Identifier  MGI:2675598 Allele Type  Spontaneous
Gene  Slc12a6 Inheritance Mode  Recessive
Strain of Origin  C3H/HeSnJ Is Recombinase  false
Is Wild Type  false
molecularNote  This spontaneous mutation arose at The Jackson Laboratory. A 17 bp deletion in exon 4 was detected through sequence analysis. Western blot analysis indicated that no detectable protein product is expressed in kidney and brain tissues.
  • mutations:
  • Intragenic deletion
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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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