Entity Details

Primary name FANCE_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9HB96
EntryNameFANCE_HUMAN
FullNameFanconi anemia group E protein
TaxID9606
Evidenceevidence at protein level
Length536
SequenceStatuscomplete
DateCreated2004-03-15
DateModified2021-06-02

Ontological Relatives

GenesFANCE

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0036297 interstrand cross-link repair
GO:0043240 Fanconi anaemia nuclear complex

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR021025 Fanconi Anaemia group E protein, C-terminalDomainDomain
IPR039685 Fanconi anemia group E proteinFamilyFamily

Diseases

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Disease IDSourceNameDescription
600901 OMIMFanconi anemia complementation group E (FANCE)A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair. The disease is caused by variants affecting the gene represented in this entry.