# Doublecortin domain containing 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q5204485](https://www.wikidata.org/wiki/Q5204485)  
**Source**: https://4ort.xyz/entity/doublecortin-domain-containing-2-q5204485


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9UHG0)
3. Q20641742
4. [DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
5. [A proteome-scale map of the human interactome network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
6. [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:Q9UHG0)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
8. [DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
9. [DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
10. [DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
12. [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?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
13. [Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
14. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
15. [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:Q9UHG0)
16. [A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
17. [DCDC2 is associated with reading disability and modulates neuronal development in the brain](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UHG0&geneProductId=UniProtKB:Q9UHG0)
18. [DCDC2 is associated with reading disability and modulates neuronal development in the brain](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UHG0)
19. Ensembl Release 99