Identity
HGNC
LOCATION
1p31.3
LOCUSID
ALIAS
SHNKND,UGTREL7
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: 23169
MIM: 610804
HGNC: 20800
Ensembl: ENSG00000116704
Variants:
dbSNP: 23169
ClinVar: 23169
TCGA: ENSG00000116704
COSMIC: SLC35D1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000116704 | ENST00000235345 | Q9NTN3 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35934917 | 2022 | A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree. | 1 |
| 35934917 | 2022 | A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree. | 1 |
| 27712858 | 2016 | Fine mapping of the GWAS loci identifies SLC35D1 and IL23R as potential risk genes for leprosy. | 3 |
| 27712858 | 2016 | Fine mapping of the GWAS loci identifies SLC35D1 and IL23R as potential risk genes for leprosy. | 3 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 19508970 | 2009 | Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases. | 17 |
| 19508970 | 2009 | Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases. | 17 |
| 17952091 | 2007 | Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human. | 49 |
| 17952091 | 2007 | Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human. | 49 |
Citation
Dessen P
SLC35D1 (solute carrier family 35 member D1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73404/slc35d1-(solute-carrier-family-35-member-d1)
