xeroderma pigmentosum group G Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

Disease Ontology Browser

xeroderma pigmentosum group G (DOID:0110849)
Alliance: disease page
Synonyms: xeroderma pigmentosum VII; XP7; XP group G; XPG
Alt IDs: OMIM:278780, ICD10CM:Q82.1
Definition: A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.

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 04/09/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Ercc5tm2Shm/Ercc5tm2Shm	involves: 129S2/SvPas * C57BL/6J	J:89911	View
Ercc5tm3Shm/Ercc5tm3Shm	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	J:89911	View
Ercc5tm4Shm/Ercc5tm4Shm	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	J:89911	View
Ercc5tm1Shm/Ercc5tm1Shm	involves: 129S2/SvPas * C57BL/6J	J:53756	View