|  Help  |  About  |  Contact Us

Allele : Spta1<sph> spectrin alpha, erythrocytic 1; spherocytosis

Primary Identifier  MGI:1856377 Allele Type  Spontaneous
Gene  Spta1 Inheritance Mode  Recessive
Strain of Origin  C3H Is Recombinase  false
Is Wild Type  false
description  This original spherocytosis mutation arose in an unpedigreed C3H stock.
molecularNote  The mutation in the sph mouse was identified as a single base pair deletion in exon 11 that causes a frame shift and premature stop codon.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • sph,
  • sph
Quick Links:
 
Quick Links:
 

1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

4 Carried By

Trail: Allele

0 Driven By

24 Publication categories

Trail: Allele