Molecular cloning of SLC26A7, a novel member of the SLC26 sulfate/anion transporter family, from high endothelial venules and kidney

Genomics

Volumn 79, Issue 2, 2002, Pages 249-256

  Vincourt, Jean Baptiste ^a   Jullien, Denis ^b   Kossida, Sophia ^a,b   Amalric, François ^a   Girard, Jean Philippe ^a  

^a CNRS   (France)

^b ENDOCUBE   (France)

Author keywords

Alternative splicing; Endothelial cells; Kidney; L selectin; Sulfate; Transporter

Indexed keywords

COMPLEMENTARY DNA; GENE PRODUCT; HOMING RECEPTOR; L SELECTIN; PROTEIN SLC26A7; SIALOMUCIN; SULFATE; UNCLASSIFIED DRUG;

ANION EXCHANGE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CHRONIC INFLAMMATION; ENDOTHELIUM CELL; GENE EXPRESSION; HUMAN; HUMAN TISSUE; KIDNEY; LYMPHOID ORGAN; MOLECULAR CLONING; MULTIGENE FAMILY; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; POLYADENYLATION; PRIORITY JOURNAL; RNA SPLICING;

EID: 0035706333     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6689     Document Type: Article

References (33)

1. Lymphocyte homing and homeostasis
2. Physiological and molecular mechanisms of lymphocyte homing
3. High endothelial venules (HEVs): Specialized endothelium for lymphocyte migration
4. Molecular cloning and functional analysis of SUT-1, a sulfate transporter from human high endothelial venules
5. Sulfation in high endothelial venules: Cloning and expression of the human PAPS synthetase
6. Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectin
7. A novel, high endothelial venule-specific sulfotransferase expresses 6-sulfo sialyl Lewis(x), an L-selectin ligand displayed by CD34
8. The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
9. Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene
10. Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 Novel mutations, mutation review, associated skeletal phenotypes, and diagnostic relevance
11. Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger
12. Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family
13. Plant members of a family of sulfate transporters reveal functional subtypes
14. Molecular characterization of two high affinity sulfate transporters in Saccharomyces cerevisiae
15. The down regulated in Adenoma (dra) gene encodes an intestine-specific membrane sulfate transport protein
16. The down-regulated in adenoma (DRA) gene encodes an intestine-specific membrane glycoprotein
17. Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea
18. Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes
19. Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling
20. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
21. Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
22. The Pendred syndrome gene encodes a chloride-iodide transport protein
23. Prestin is the motor protein of cochlear outer hair cells
24. Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein
25. Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells
26. The STAS domain - A link between anion transporters and antisigma-factor antagonists
27. Oxalate transport via the sulfate/HCO3 exchanger in rabbit renal basolateral membrane vesicles
28. Pathways for oxalate transport in rabbit renal microvillus membrane vesicles
29. Immunolocalization of sat-1 sulfate/oxalate/bicarbonate anion exchanger in the rat kidney
30. Expression of rat renal sulfate transport systems in Xenopus laevis oocytes. Functional characterization and molecular identification
31. Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): Evidence for a phenotypic series involving three chondrodysplasias
32. Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for an L483P substitution in the diastrophic dysplasia sulfate transporter
33. Using genewise in the Drosophila annotation experiment