Identity
HGNC
LOCATION
4q31.22
LOCUSID
ALIAS
C4orf13,P7,SSASKS
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: 84068
MIM: 611459
HGNC: 23088
Ensembl: ENSG00000120519
Variants:
dbSNP: 84068
ClinVar: 84068
TCGA: ENSG00000120519
COSMIC: SLC10A7
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38037133 | 2023 | Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine. | 0 |
| 38037133 | 2023 | Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine. | 0 |
| 34999954 | 2022 | SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation. | 1 |
| 34999954 | 2022 | SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation. | 1 |
| 33561315 | 2021 | Circular RNA circHECTD1 facilitates glioma progression by regulating the miR-296-3p/SLC10A7 axis. | 9 |
| 33561315 | 2021 | Circular RNA circHECTD1 facilitates glioma progression by regulating the miR-296-3p/SLC10A7 axis. | 9 |
| 32350310 | 2020 | The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling. | 11 |
| 32350310 | 2020 | The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling. | 11 |
| 29878199 | 2018 | Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation. | 22 |
| 30082715 | 2018 | SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. | 19 |
| 29878199 | 2018 | Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation. | 22 |
| 30082715 | 2018 | SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. | 19 |
| 19240061 | 2009 | Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. | 94 |
| 19240061 | 2009 | Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. | 94 |
| 17628207 | 2007 | Molecular and phylogenetic characterization of a novel putative membrane transporter (SLC10A7), conserved in vertebrates and bacteria. | 17 |
Citation
Dessen P
SLC10A7 (solute carrier family 10 member 7)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73275/slc10a7-(solute-carrier-family-10-member-7)
