About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3655827
Allelic
Composition
Foxc1tm1Blh/Foxc1+
Genetic
Background
B6.Cg-Foxc1tm1Blh
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxc1tm1Blh mutation (0 available); any Foxc1 mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• pigmented mice had mild developmental defects than compared to albino Tyrc-2J/Tyrc-2J, Foxc1tm1Blh /Foxc1+ mice (J:82280)
• pigmented mice had mild developmental defects than compared to albino Tyrc-2J/Tyrc-2J, Foxc1tm1Blh /Foxc1+ mice (J:82280)
• mild hypoplasia (J:82280)
• mild hypoplasia (J:82280)

Mouse Models of Human Disease
OMIM ID Ref(s)
Glaucoma 3, Primary Congenital, A; GLC3A 231300 J:82280


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/02/2016
MGI 6.02
The Jackson Laboratory