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Allele : Hprt1<tm2(AGT)Sig> hypoxanthine phosphoribosyltransferase 1; targeted mutation 2, Curt Sigmund

Primary Identifier  MGI:2449453 Allele Type  Targeted
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Hprt1
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  The entire human AGT genomic sequence containing a C to T nucleotide substitution at codon 235 was inserted into the Hprt locus via homologous recombination. (This polymorphism results in a threonine to methionine substitution and has been reported in association with hypertension in humans.) Northern blot analysis showed high transgene expression in liver and kidneys, and lower levels of transgene expression in brain, white and brown adipose tissue, diaphram, and aorta. In addition, immunohistochemical analysis of kidney and liver sections detected transgene expression in the proximal tubule cells of the renal cortex and in hepatocytes.
  • mutations:
  • Insertion
  • synonyms:
  • hAGT<GM>,
  • hAGT<GM>,
  • hAGT<hprt>,
  • hAGT<hprt>
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1 Feature

Genome

1 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories