About   Help   FAQ
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)





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory