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Allele : Slc39a8<tm1.1Brvo> solute carrier family 39 (metal ion transporter), member 8; targeted mutation 1.1, Bruno Vogt

Primary Identifier  MGI:7541328 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Slc39a8
Transmission  Germline Strain of Origin  C57BL/6
Is Recombinase  false Is Wild Type  false
molecularNote  Alanine codon 393 (GCT) in exon 7 was changed to threonine (ACT) (p.A393T) and an FRT site flanked neomycin resistance gene cassette was inserted into intron 8. The neo cassette was removed through subsequent Flp-mediated recombination. The mutation is the equivalent of the human p.A391T mutation (SNP rs13107325) associated with numerous traits, including reduced arterial blood pressure, increased body mass index and hyperlipidemia.
  • mutations:
  • Single point mutation
  • synonyms:
  • ZIP8 A393T,
  • ZIP8 A393T,
  • ZIP8KI,
  • ZIP8KI
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories