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

Symbol:	Tc-3H
Name:	brachyury, T-box transcription factor T; curtailed 3 Harwell
MGI ID:	MGI:3042264
Gene:	T  Location: Chr17:8653255-8661328 bp, + strand  Genetic Position: Chr17, 4.92 cM
Alliance:	Tc-3H page

Strain of Origin:

BALB/cOlaHsd

Allele Type:    Chemically induced (ENU) Mutation:    Nucleotide substitutions   Mutation details: The Tc-3H allele is caused by a splice donor mutation at the end of exon 7. A protein truncation, either due to exon skipping or to read-through of the donor site causing an altered open reading frame beyond amino acid 344, is predicted. (J:93195) Inheritance:    Semidominant

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

In Structures Affected by this Mutation:

1 anatomical structure(s)

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:	60 strains or lines available

Original:	J:93195 Bogani D, et al., New semidominant mutations that affect mouse development. Genesis. 2004 Oct;40(2):109
All:	1 reference(s)