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

Symbol:	Tgm3we
Name:	transglutaminase 3, E polypeptide; wellhaarig
MGI ID:	MGI:1856269
Gene:	Tgm3  Location: Chr2:129854269-129892319 bp, + strand  Genetic Position: Chr2, 63.19 cM
Alliance:	Tgm3we page

Strain of Origin:

Agnes Bluhm's stocks

Allele Type:    Spontaneous Mutation:    Single point mutation   Mutation details: A spontaneous C-to-T point mutation in exon 13 results in premature termination codon at arginine 658 (p.R658*) and the loss of the last 36 amino acids. There is also an insertion/duplication of AGTC in intron 12 between position chr2:130048178-130048179 (GRCm38) (duplication of 130048179-130048182). (J:225940) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

3 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 6 strains available      Cell Lines: 0 lines available
Carrying any Tgm3 Mutation:	53 strains or lines available

Original:	J:208 Hertwig P, Neue Mutationen und Koppelungsgruppen bei der Hausmaus. Z Indukt Abstamm Vererbungsl. 1942;80(1):220-246
All:	11 reference(s)