Entity Details

Primary name WDR72
Entity type gene
Source Source Link

Details

PrimaryID256764
RefseqGeneNG_017034
SymbolWDR72
NameWD repeat domain 72
Chromosome15
Location15q21.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-07-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsWDR72_HUMAN

GO terms

Show/Hide Table
GOName
GO:0005737 cytoplasm
GO:0031214 biomineral tissue development
GO:0031410 cytoplasmic vesicle

Diseases

Show/Hide Table
Disease IDSourceNameDescription
613211 OMIMAmelogenesis imperfecta, hypomaturation type, 2A3 (AI2A3)A defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
WDR72SMARCA2BioGRID31753913 details