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th17
Spontaneous Allele Detail
Summary
Symbol: th17
Name: t-complex; t, Harwell 17
MGI ID: MGI:1856737
Gene: t  Location: unknown  Genetic Position: Chr17, Syntenic
Alliance: th17 page
Mutation
origin
Strain of Origin:  STOCK T +/t6 T(1;17)190Ca
Mutation
description
Allele Type:    Spontaneous
Mutation:    Deletion
  th17 involves 1 genes/genome features (t) View all
 
Mutation detailsThis allele is a derivative of the t6 haplotype, missing the proximal end but retaining the distal end including the recessive lethal factor of t6 and is linked to the Chr 17 breakpoint in the reciprocal translocation T(1;17)190Ca. The breakpoint is within a crossover-suppression region therefore th17 can not be separated from the translocation. (J:5889)
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 t Mutation:  19 strains or lines available
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:  7 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
10/22/2024
MGI 6.24
The Jackson Laboratory