Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | References

Symbol:	th17
Name:	t-complex; t, Harwell 17
MGI ID:	MGI:1856737
Gene:	t  Location: unknown  Genetic Position: Chr17, Syntenic
Alliance:	th17 page

Strain of Origin:

STOCK T +/t6 T(1;17)190Ca

Allele Type:    Spontaneous Mutation:    Deletion   th17 involves 1 genes/genome features (t) View all   Mutation details: This 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

View phenotypes and curated references for all genotypes (concatenated display).

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

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)