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Tcirg1oc
Spontaneous Allele Detail
Summary
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.

Mutation
origin
Strain of Origin:  C57BL/6J-Vps33abf
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThis 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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 3 assay results
In Structures Affected by this Mutation: 12 anatomical structure(s)
Find Mice (IMSR)
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:  36 strains or lines available
References
Original:  J:28464 Dickie MM, Osteosclerotic (oc). Mouse News Lett. 1967;36:39
All:  25 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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory