retinitis pigmentosa 28 Disease Ontology Browser

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Disease Ontology Browser

retinitis pigmentosa 28 (DOID:0110365)
Alliance: disease page
Synonyms: RP28
Alt IDs: OMIM:606068, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the FAM161A gene on chromosome 2p15.

Disease References using Mouse Models (1)

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 04/09/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Fam161aGt(462E7)Cmhd/Fam161aGt(462E7)Cmhd	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	J:214319	View