Leber congenital amaurosis 8 Disease Ontology Browser

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Disease Ontology Browser

Leber congenital amaurosis 8 (DOID:0110079)
Alliance: disease page
Synonyms: LCA8
Alt IDs: OMIM:613835, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32.

Disease References using Mouse Models (2)

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 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Crb1rd8/Crb1rd8	STOCK Crb1^rd8/J	J:171736	View
Crb1tm1Wij/Crb1tm1Wij Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL	J:207895	View
Crb1tm1Wij/Crb1+ Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL	J:207895	View