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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cux2Gt(OST440231)Lex
gene trap OST440231, Lexicon Genetics
MGI:4353153
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cux2Gt(OST440231)Lex/Cux2Gt(OST440231)Lex involves: 129S5/SvEvBrd MGI:4353225


Genotype
MGI:4353225
hm1
Allelic
Composition
Cux2Gt(OST440231)Lex/Cux2Gt(OST440231)Lex
Genetic
Background
involves: 129S5/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cux2Gt(OST440231)Lex mutation (0 available); any Cux2 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous pups are produced at less than expected frequency

nervous system
• hypoplastic at E11.5
• area of tube reduced 27.8%
• marginal zone is reduced (J:131816)
• reduced axonal mass in the marginal zone (J:131816)
• hypoplastic at E11.5 (J:150348)
• 40-60% reduction of various interneuron types
• reduced commissural interneurons
• reduced axonal projections from interneurons
• abnormal ventral root formation

cellular
• 62% increase in the length of time neural progenitors spend in S phase
• slower cell cycle
• proliferation level normal at E10.5
• reduced neural progenitor cell proliferation at E11.5

embryo
• hypoplastic at E11.5
• area of tube reduced 27.8%
• marginal zone is reduced (J:131816)
• reduced axonal mass in the marginal zone (J:131816)
• hypoplastic at E11.5 (J:150348)





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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