Entity Details

Primary name WDR45B
Entity type gene
Source Source Link

Details

PrimaryID56270
RefseqGeneNG_046895
SymbolWDR45B
NameWD repeat domain 45B
Chromosome17
Location17q25.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-08-26
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsWIPI3_HUMAN

GO terms

Show/Hide Table
GOName
GO:0000045 autophagosome assembly
GO:0000407 phagophore assembly site
GO:0000422 autophagy of mitochondrion
GO:0005764 lysosome
GO:0005829 cytosol
GO:0006497 protein lipidation
GO:0009267 cellular response to starvation
GO:0019898 extrinsic component of membrane
GO:0032266 phosphatidylinositol-3-phosphate binding
GO:0034045 phagophore assembly site membrane
GO:0034497 protein localization to phagophore assembly site
GO:0044804 autophagy of nucleus
GO:0062078 TSC1-TSC2 complex binding
GO:0080025 phosphatidylinositol-3,5-bisphosphate binding

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617977 OMIMNeurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures (NEDSBAS)An autosomal recessive disorder characterized by profound developmental delay, progressive spastic quadriplegia and contractures, early-onset refractory epilepsy in most patients, and brain malformations. Neuroimaging shows ventriculomegaly, reduced cerebral white matter volume, and thinning of cerebral gray matter. The disease may be caused by variants affecting the gene represented in this entry.