Entity Details

Primary name ZN687_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N1G0
EntryNameZN687_HUMAN
FullNameZinc finger protein 687
TaxID9606
Evidenceevidence at protein level
Length1237
SequenceStatuscomplete
DateCreated2006-05-02
DateModified2021-06-02

Ontological Relatives

GenesZNF687

GO terms

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GOName
GO:0003677 DNA binding
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR013087 Zinc finger C2H2-typeDomainDomain
IPR036236 Zinc finger C2H2 superfamilyFamilyHomologous superfamily
IPR041697 Zinc-finger C2H2-type 11DomainDomain

Diseases

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Disease IDSourceNameDescription
616833 OMIMPaget disease of bone 6 (PDB6)An autosomal dominant form of Paget disease, a disorder of bone remodeling characterized by increased bone turnover affecting one or more sites throughout the skeleton, primarily the axial skeleton. Osteoclastic overactivity followed by compensatory osteoblastic activity leads to a structurally disorganized mosaic of bone (woven bone), which is mechanically weaker, larger, less compact, more vascular, and more susceptible to fracture than normal adult lamellar bone. PDB6 is characterized by adult onset of bone pain associated with polyostotic bone lesions primarily affecting the axial skeleton. In some cases, the pagetic tissue undergoes neoplastic transformation, resulting in osteosarcoma and, less frequently, in giant cell tumor of bone. The disease is caused by variants affecting the gene represented in this entry.