xeroderma pigmentosum group F Disease Ontology Browser

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Disease Ontology Browser

xeroderma pigmentosum group F (DOID:0110848)
Alliance: disease page
Synonyms: xeroderma pigmentosum VI; XP6; XP group F; XPF
Alt IDs: OMIM:278760, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13.

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 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Ercc4tm1Fwa/Ercc4tm1Fwa	involves: 129S6/SvEvTac	J:87684	View