Identity
HGNC
LOCATION
6p22.3
LOCUSID
ALIAS
DCDC2A,DFNB66,NPHP19,NSC,RU2,RU2S
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 51473
MIM: 605755
HGNC: 18141
Ensembl: ENSG00000146038
Variants:
dbSNP: 51473
ClinVar: 51473
TCGA: ENSG00000146038
COSMIC: DCDC2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000146038 | ENST00000378450 | Q9UHG0 |
| ENSG00000146038 | ENST00000378454 | Q9UHG0 |
| ENSG00000146038 | ENST00000436313 | H0Y784 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38610086 | 2024 | Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults. | 0 |
| 38658618 | 2024 | DCDC2 inhibits hepatic stellate cell activation and ameliorates CCl(4)-induced liver fibrosis by suppressing Wnt/β-catenin signaling. | 0 |
| 38610086 | 2024 | Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults. | 0 |
| 38658618 | 2024 | DCDC2 inhibits hepatic stellate cell activation and ameliorates CCl(4)-induced liver fibrosis by suppressing Wnt/β-catenin signaling. | 0 |
| 36938759 | 2023 | Biallelic known and novel DCDC2 variants in cholestatic liver disease: Phenotype-genotype observations in four children. | 0 |
| 36938759 | 2023 | Biallelic known and novel DCDC2 variants in cholestatic liver disease: Phenotype-genotype observations in four children. | 0 |
| 34873813 | 2022 | Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance. | 2 |
| 34873813 | 2022 | Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance. | 2 |
| 34155636 | 2021 | Two cases of DCDC2-related neonatal sclerosing cholangitis with developmental delay and literature review. | 3 |
| 34186533 | 2021 | Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young Children. | 3 |
| 34228165 | 2021 | White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant. | 5 |
| 34155636 | 2021 | Two cases of DCDC2-related neonatal sclerosing cholangitis with developmental delay and literature review. | 3 |
| 34186533 | 2021 | Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young Children. | 3 |
| 34228165 | 2021 | White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant. | 5 |
| 31411106 | 2020 | Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes. | 4 |
Citation
Dessen P
DCDC2 (doublecortin domain containing 2)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/40269/dcdc2
