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Allele : Ahsp<tm2.1Mjwe> alpha hemoglobin stabilizing protein; targeted mutation 2.1, Mitchell J Weiss

Primary Identifier  MGI:7517218 Allele Type  Targeted
Gene  Ahsp Transmission  Germline
Strain of Origin  129S/SvEv Is Recombinase  false
Is Wild Type  false
molecularNote  Proline codon 30 (CCT) in exon 3 was changed to alanine (GCT) (p.P30A) and a loxP site flanked neomycin resistance gene cassette was inserted into intron 2. The neo cassette was removed through subsequent Cre-mediated recombination. The affected residue is located in loop 1, between helix 1 and 2, of the encoded peptide and is thought to be involved in oxygenated alpha-globin binding.
  • mutations:
  • Single point mutation
  • synonyms:
  • Ahsp<P30A>,
  • Ahsp<P30A>
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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

3 Publication categories

Trail: Allele