xeroderma pigmentosum group E Disease Ontology Browser

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Disease Ontology Browser

xeroderma pigmentosum group E (DOID:0110846)
Alliance: disease page
Synonyms: xeroderma pigmentosum V; XP5; XP group E; XPE
Alt IDs: OMIM:278740, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by a mild phenotype that has_material_basis_in homozygous mutation in the DDB2 gene on chromosome 11p11.

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
Ddb2tm1Linn/Ddb2tm1Linn	involves: 129S/SvEv * C57BL/6	J:88125	View
Ddb2tm1Pra/Ddb2tm1Pra	involves: C57BL/6	J:95633	View
Ddb2tm1Linn/Ddb2+	involves: 129S/SvEv * C57BL/6	J:88125	View
Ddb2tm1Pra/Ddb2+	involves: C57BL/6	J:95633	View