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Allele : Spta1<sph-ha> spectrin alpha, erythrocytic 1; hemolytic anemia

Primary Identifier  MGI:1856181 Allele Type  Spontaneous
Gene  Spta1 Inheritance Mode  Recessive
Strain of Origin  DBA/1J Is Recombinase  false
Is Wild Type  false
molecularNote  The mutation in the sph-ha mouse (also known as sph-J) was identified as a C-to-A transversion in exon 52 that converts a tyrosine 2403 to a stop codon (p.Y2403*). This mutation truncates the protein by 13 amino acids.
  • mutations:
  • Single point mutation
  • synonyms:
  • Sph-J,
  • ha,
  • sph<1J>,
  • Sph-J,
  • sph<1J>,
  • ha
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

20 Publication categories