About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nxnl2tm1.2Tlev
targeted mutation 1.2, Thierry Leveillard
MGI:5426260
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nxnl2tm1.2Tlev/Nxnl2tm1.2Tlev BALB/c-Nxnl2tm1.2Tlev MGI:5426266


Genotype
MGI:5426266
hm1
Allelic
Composition
Nxnl2tm1.2Tlev/Nxnl2tm1.2Tlev
Genetic
Background
BALB/c-Nxnl2tm1.2Tlev
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxnl2tm1.2Tlev mutation (0 available); any Nxnl2 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• reduced S- and M-cone densities at 10 months
• at 10 months, mice exhibit reduced photopic electroretinogram of b-wave amplitude compared with wild-type mice
• however, expression of the short trophic isoform rescues cone electrophysiology
• at 10 months, mice exhibit decreased a-wave amplitudes compared with wild-type mice

taste/olfaction
• impaired olfactory discrimination with age

nervous system
• reduced S- and M-cone densities at 10 months

craniofacial

respiratory system

growth/size/body





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
10/29/2024
MGI 6.24
The Jackson Laboratory