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Spta1sph-2J
Spontaneous Allele Detail
Summary
Symbol: Spta1sph-2J
Name: spectrin alpha, erythrocytic 1; spherocytosis 2 Jackson
MGI ID: MGI:1858128
Synonyms: sph2J
Gene: Spta1  Location: Chr1:174000342-174076016 bp, + strand  Genetic Position: Chr1, 80.97 cM
Alliance: Spta1sph-2J page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Spta1 Mutation:  147 strains or lines available
Notes
Spna1sph-2J, spherocytosis-2J, recessive. This mutation arose in the C3HeB/FeJ strain. It resembles Spna1sph in the absence of a-spectrin in the red cell membrane skeleton (J:12205) . This allele is extinct (J:88022).
References
Original:  J:7501 Bodine DM 4th, et al., Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes. Cell. 1984 Jul;37(3):721-9
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory