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th20
Spontaneous Allele Detail
Summary
Symbol: th20
Name: t-complex; t, Harwell 20
MGI ID: MGI:1856739
Gene: t  Location: unknown  Genetic Position: Chr17, Syntenic
Alliance: th20 page
Mutation
origin
Strain of Origin:  STOCK T Itpr3tf/t6 +
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intergenic deletion
 
Mutation detailsThis t-haplotype is derived from t6 and involves a deletion. Breeding experiments show that it deletes tf, Kb and tw5. Southern analysis shows it also deletes Hba-ps4. (J:7337, J:7346)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 t Mutation:  19 strains or lines available
Notes
This allele is the result of a cross-over event between T and tf but retained the recessive lethality of its parent haplotype t<6>.
References
Original:  J:5889 Lyon MF, et al., Derivation of mutant t-haplotypes of the mouse by presumed duplication or deletion. Genet Res. 1977 Aug;30(1):63-76
All:  5 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
03/19/2024
MGI 6.23
The Jackson Laboratory