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Allele : Slc30a8<tm1.1Vlcg> solute carrier family 30 (zinc transporter), member 8; targeted mutation 1.1, Velocigene

Primary Identifier  MGI:6197055 Allele Type  Targeted
Attribute String  Humanized sequence, Null/knockout Gene  Slc30a8
Transmission  Germline Strain of Origin  C57BL/6NTac
Is Recombinase  false Is Wild Type  false
molecularNote  Nucleotide 409 was changed from a C to T in exon 3 and a self-excising neo cassette was inserted in intron 3 deleting 23 bp of sequence via homologous recombination. The mutation in exon 3 changes an arginine into a stop codon. RNA in situ hybridization showed a 70% reduction in mRNA expression in pancreatic islets from homozygous mice. However, western blot analysis failed to detect any protein in this tissue in homozygous mice. This mutation is analogous to the human p.Arg138* variant.
  • mutations:
  • Single point mutation,
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Slc30a8 R138X,
  • Slc30a8 R138X
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

5 Publication categories

Trail: Allele