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: 9187
MIM: 603617
HGNC: 10975
Ensembl: ENSG00000074621
Variants:
dbSNP: 9187
ClinVar: 9187
TCGA: ENSG00000074621
COSMIC: SLC24A1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 26822852 | 2016 | Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness. | 8 |
| 27624628 | 2016 | Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations. | 34 |
| 26822852 | 2016 | Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness. | 8 |
| 27624628 | 2016 | Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations. | 34 |
| 20850105 | 2010 | A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness. | 36 |
| 20850105 | 2010 | A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness. | 36 |
Citation
Dessen P
SLC24A1 (solute carrier family 24 member 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73328/slc24a1-(solute-carrier-family-24-member-1)
