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

Symbol: Tcirg1oc Name: T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3; osteosclerotic MGI ID: MGI:1856973 Synonyms: Atp6i-, oc Gene: Tcirg1  Location: Chr19:3946050-3957133 bp, - strand  Genetic Position: Chr19, 3.62 cM Alliance: Tcirg1oc page

Tcirg1oc/Tcirg1oc and control Show the 1 phenotype image(s) involving this allele.

Strain of Origin:

C57BL/6J-Vps33abf

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Mutation details: This mutation was defined as a 1579 bp deletion starting in the middle of intron 1 and extending 62 bp into exon 3. (J:61295) Inheritance:    Recessive

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

In Mice Carrying this Mutation:	3 assay results
In Structures Affected by this Mutation:	12 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Tcirg1 Mutation:	35 strains or lines available

Original:	J:28464 Dickie MM, Osteosclerotic (oc). Mouse News Lett. 1967;36:39
All:	25 reference(s)