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Allele : Slc26a4<pdsm> solute carrier family 26, member 4; Pendred's syndrome model
Primary Identifier  MGI:3693973 Allele Type  Spontaneous
Gene  Slc26a4 Inheritance Mode  Recessive
Strain of Origin  BXA7/PgnJ Is Recombinase  false
Is Wild Type  false
molecularNote  A T-to-A transversion occurred spontaneously in exon 7 resulting in the introduction of a premature stop codon at cysteine codon 282 (p.C282*).
  • mutations:
  • Single point mutation
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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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