cataract 39 multiple types Disease Ontology Browser

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Disease Ontology Browser

cataract 39 multiple types (DOID:0110236)
Alliance: disease page
Synonyms: autosomal dominant cataract 39 multiple types; CTRCT39
Alt IDs: OMIM:615188, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34.

Disease References using Mouse Models (3)

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, Copyright, and Privacy Statement Send questions and comments to User Support.	last database update 01/24/2023 MGI 6.22

Allelic Composition	Genetic Background	Reference	Phenotypes
CrygbNop/CrygbNop	Not Specified	J:7589	View
CrygbClapper/CrygbClapper	C57BL/6J-Crygb^Clapper	J:100851	View
CrygbS11R/CrygbS11R	A/J-Crygb^S11R	J:132502	View
CrygbNop/Crygb+	Not Specified	J:7589	View
CrygbClapper/Crygb+	C57BL/6J-Crygb^Clapper	J:100851	View
CrygbS11R/Crygb+	A/J-Crygb^S11R	J:132502	View