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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc
targeted mutation 5, Mario R Capecchi
MGI:5649273
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc/Gt(ROSA)26Sortm1(cre/ERT)Nat involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5649275
cn2
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc/Gt(ROSA)26Sor+
Tg(Prrx1-cre/ERT2)1Mlgn/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5649279


Genotype
MGI:5649275
cn1
Allelic
Composition
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc/Gt(ROSA)26Sortm1(cre/ERT)Nat
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(cre/ERT)Nat mutation (3 available); any Gt(ROSA)26Sor mutation (944 available)
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc mutation (0 available); any Gt(ROSA)26Sor mutation (944 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice develop a tumor within the skull between 3 and 6 months of age; tumors are found primarily in the brain parenchyma, but also in the choroid plexus and orbit
• tumors show characteristic nests of polygonal cells with an open chromatin pattern, surrounded by neatly arcading capillary and larger vascular channels, resembling alveolar soft part sarcoma
• tumors often arise in or near the leptomeninges, along sulci
• some tumors show aggressive invasive growth, with extensions of tumor cells into the cerebellum, cerebrum, and the vessels of the choroid plexus
• mice do not develop tumors in the skeletal muscle
• tumors form in the areas highest in lactate, the cranial vault, express high levels of lactate importers, have abundant mitochondria, metabolize lactate as a metabolic substrate, and respond to exogenous lactate administration with increased cell proliferation and angiogenesis

craniofacial
• mice often exhibit enlargement of the occipital bone from the inner soft tissue expansion

skeleton
• mice often exhibit enlargement of the occipital bone from the inner soft tissue expansion

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
alveolar soft part sarcoma DOID:4239 OMIM:606243
J:217462




Genotype
MGI:5649279
cn2
Allelic
Composition
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc/Gt(ROSA)26Sor+
Tg(Prrx1-cre/ERT2)1Mlgn/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm5(ASPSCR1/TFE3)Mrc mutation (0 available); any Gt(ROSA)26Sor mutation (944 available)
Tg(Prrx1-cre/ERT2)1Mlgn mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice develop intracranial tumors 10-14 weeks after tamoxifen treatment at 2 weeks of age
• tumors are located either within the brain parenchyma or it the periosteum along the inner table of the cranium
• however, no tumors are seen in the outer table periosteum or the limbs





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
05/14/2024
MGI 6.23
The Jackson Laboratory