# Doublecortin domain containing 2

> mammalian protein found in Rattus norvegicus

**Wikidata**: [Q28558030](https://www.wikidata.org/wiki/Q28558030)  
**Source**: https://4ort.xyz/entity/doublecortin-domain-containing-2


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/D3ZR10)
3. Q20641742
4. [Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
5. [GOA](http://www.ebi.ac.uk/QuickGO/GAnnotation?protein=D3ZR10)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
7. [A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation](http://www.ebi.ac.uk/QuickGO/GAnnotation?protein=D3ZR10)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
9. [A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
10. [DCDC2 is associated with reading disability and modulates neuronal development in the brain](http://www.ebi.ac.uk/QuickGO/GAnnotation?protein=D3ZR10)
11. [DCDC2 is associated with reading disability and modulates neuronal development in the brain](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
12. [Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:D3ZR10)
13. ensembl Release 106