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: 2298
MIM: 601092
HGNC: 3805
Ensembl: ENSG00000170122
Variants:
dbSNP: 2298
ClinVar: 2298
TCGA: ENSG00000170122
COSMIC: FOXD4
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000170122 | ENST00000382500 | Q12950 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 22876580 | 2012 | Pure distal 9p deletion in a female infant with cerebral palsy. | 1 |
| 22876580 | 2012 | Pure distal 9p deletion in a female infant with cerebral palsy. | 1 |
| 17273782 | 2007 | A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality. | 14 |
| 17273782 | 2007 | A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality. | 14 |
Citation
Dessen P
FOXD4 (forkhead box D4)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/47221/foxd4-(forkhead-box-d4)
