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: 115111
MIM: 608479
HGNC: 14467
Ensembl: ENSG00000147606
Variants:
dbSNP: 115111
ClinVar: 115111
TCGA: ENSG00000147606
COSMIC: SLC26A7
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34593695 | 2021 | Relationships between SLC26A7 expressions and extra-thyroid metastasis of papillary thyroid carcinoma. | 0 |
| 34944008 | 2021 | Alterations in SLC4A2, SLC26A7 and SLC26A9 Drive Acid-Base Imbalance in Gastric Neuroendocrine Tumors and Uncover a Novel Mechanism for a Co-Occurring Polyautoimmune Scenario. | 5 |
| 34593695 | 2021 | Relationships between SLC26A7 expressions and extra-thyroid metastasis of papillary thyroid carcinoma. | 0 |
| 34944008 | 2021 | Alterations in SLC4A2, SLC26A7 and SLC26A9 Drive Acid-Base Imbalance in Gastric Neuroendocrine Tumors and Uncover a Novel Mechanism for a Co-Occurring Polyautoimmune Scenario. | 5 |
| 32726161 | 2020 | SLC26A7 constitutes the thiocyanate-selective anion conductance of the basolateral membrane of the retinal pigment epithelium. | 2 |
| 32726161 | 2020 | SLC26A7 constitutes the thiocyanate-selective anion conductance of the basolateral membrane of the retinal pigment epithelium. | 2 |
| 29546359 | 2018 | Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis. | 26 |
| 30333321 | 2018 | Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. | 26 |
| 29546359 | 2018 | Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis. | 26 |
| 30333321 | 2018 | Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. | 26 |
| 16524946 | 2006 | Chloride/bicarbonate exchanger SLC26A7 is localized in endosomes in medullary collecting duct cells and is targeted to the basolateral membrane in hypertonicity and potassium depletion. | 17 |
| 16524946 | 2006 | Chloride/bicarbonate exchanger SLC26A7 is localized in endosomes in medullary collecting duct cells and is targeted to the basolateral membrane in hypertonicity and potassium depletion. | 17 |
| 15956810 | 2005 | SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney. | 6 |
| 15956810 | 2005 | SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney. | 6 |
| 11829495 | 2002 | Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney. | 7 |
Citation
Dessen P
SLC26A7 (solute carrier family 26 member 7)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73375/slc26a7-(solute-carrier-family-26-member-7)
