Oxalat-Transporter SLC26A6
Der Oxalat-Transporter SLC26A6 is möglicherweise für das Syndrom der Hyperoxalurie mit Diarrhoe verantwortlich sein.
Gentests:
Forschung |
Untersuchungsmethoden |
Familienuntersuchung |
Bearbeitungszeit |
5 Tage |
Probentyp |
genomische DNS |
Verknüpfte Erkrankungen:
Referenzen:
1. |
Jiang Z et al. (2006) Calcium oxalate urolithiasis in mice lacking anion transporter Slc26a6.
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2. |
None (2006) A key stone cop regulates oxalate homeostasis.
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3. |
None (2009) Recent advances in the pathophysiology of nephrolithiasis.
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4. |
Lohi H et al. (2000) Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger.
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5. |
Waldegger S et al. (2001) Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family.
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6. |
Chernova MN et al. (2005) Functional comparison of mouse slc26a6 anion exchanger with human SLC26A6 polypeptide variants: differences in anion selectivity, regulation, and electrogenicity.
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7. |
Markovich D et al. (2007) Specificity and regulation of renal sulfate transporters.
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8. |
Soleimani M et al. (2006) SLC26 chloride/base exchangers in the kidney in health and disease.
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9. |
None (2006) Overview of the SLC26 family and associated diseases.
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10. |
Sindić A et al. (2007) Renal physiology of SLC26 anion exchangers.
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11. |
NCBI article
NCBI 65010
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12. |
OMIM.ORG article
Omim 610068
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Update: 14. August 2020