Fanconi anemia complementation group T Disease Ontology Browser

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Disease Ontology Browser

Fanconi anemia complementation group T (DOID:0111081)
Alliance: disease page
Synonyms: FANCT
Alt IDs: OMIM:616435
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.

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)
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