# WD repeat domain 62

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21105817](https://www.wikidata.org/wiki/Q21105817)  
**Source**: https://4ort.xyz/entity/wd-repeat-domain-62


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O43379)
3. Q20641742
4. [Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
5. [A proteome-scale map of the human interactome network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
6. [Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
7. [A human interactome in three quantitative dimensions organized by stoichiometries and abundances](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
8. [Towards a proteome-scale map of the human protein–protein interaction network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43379&geneProductId=UniProtKB:O43379)
10. [Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43379&geneProductId=UniProtKB:O43379)
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
12. [Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43379&geneProductId=UniProtKB:O43379)
13. [WDR62 is associated with the spindle pole and is mutated in human microcephaly](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43379&geneProductId=UniProtKB:O43379)
14. [WDR62 is associated with the spindle pole and is mutated in human microcephaly](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
15. [Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
16. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
17. [Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
18. [Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex](http://www.ebi.ac.uk/QuickGO/annotations?protein=O43379&geneProductId=UniProtKB:O43379)
19. [Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O43379)
20. Ensembl Release 99