Human Disease and Mouse Model Detail

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Human Disease

Glaucoma 3, Primary Congenital, A; GLC3A
OMIM ID: 231300

Synonyms

Glaucoma, Congenital; GLC3

View all models

View ALL (7) mouse models for this human disease.

Genes and
mouse models

Mutations in human and/or mouse homologs are associated with this disease

*Gene is associated with the disease in this species
Mouse Homologs	Human Homologs	Mouse Models	Mouse : Human Homology Class
Cyp1b1*	CYP1B1*	View 4 models	1:1 Homology
Foxc1*	FOXC1	View 2 models	1:1 Homology
Tyr*	TYR	View 3 models	1:1 Homology

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 05/08/2013 MGI 5.13

Allelic Composition	Genetic Background	Reference	Phenotypes
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz	129X1.Cg-Cyp1b1tm1Gonz	J:82280	View
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz	B6.Cg-Cyp1b1tm1Gonz	J:82280	View
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz Tyrc-2J/Tyrc-2J	B6.Cg-Tyrc-2J Cyp1b1tm1Gonz	J:82280	View
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz	involves: 129X1/SvJ * C57BL/6J	J:82280	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Tyrc-2J/Tyrc-2J	B6(Cg)-Tyrc-2J/J	J:82280	View
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz Tyrc-2J/Tyrc-2J	B6.Cg-Tyrc-2J Cyp1b1tm1Gonz	J:82280	View
Foxc1tm1Blh/Foxc1⁺ Tyrc-2J/Tyrc-2J	B6.Cg-Tyrc-2J Foxc1tm1Blh	J:82280	View