t<h17> Spontaneous Allele Detail MGI Mouse (MGI:1856737)

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t^h17
Spontaneous Allele Detail

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

Summary

Symbol:	t^h17
Name:	t-complex; t, Harwell 17
MGI ID:	MGI:1856737
Gene:	t Location: unknown Genetic Position: Chr17, Syntenic
Alliance:	t^h17 page

Mutation
origin

Strain of Origin:

STOCK T +/t⁶ T(1;17)190Ca

Mutation
description

Allele Type:		Spontaneous
Mutation:		Deletion
		t^h17 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 t^h17 can not be separated from the translocation. (J:5889)
Inheritance:		Recessive

Phenotypes

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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