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Phenotypes Associated with This Genotype
Genotype
MGI:3029012
Allelic
Composition
Smarcc1tm1Rhs/Smarcc1+
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Smarcc1tm1Rhs mutation (0 available); any Smarcc1 mutation (69 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• ectopic proliferating and differentiating cells were noted in the upper posterior region, and the cells were reduced in number in the telencephalic striatum region
• extensive malformations in embryos exhibiting exencephaly; expansion of the corpus striatum mediale
• described as malformed
• open third ventricle
• epithelia were located below the thalamus; ganglionic eminence appeared rotated towards the midline
• 20% of heterozygous embryos exhibit exencephaly

embryo
• in some embryos exhibit failure of neural fold elevation resulting in failure of neural plate closing and an abnormal brain structure
• ectopic proliferating and differentiating cells were noted in the upper posterior region, and the cells were reduced in number in the telencephalic striatum region


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
04/09/2024
MGI 6.23
The Jackson Laboratory