SLC26A3 wt Allele
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SLC26A3 wt Allele Definition
Human SLC26A3 wild-type allele is located within 7q31and is approximately 38 kb in length. This allele, which encodes chloride anion exchanger protein, plays a role in the mediation of electrolyte and fluid absorption. Defects in the SLC26A3 gene produce variant alleles that are the cause of congenital chloride diarrhea (CLD).
SLC26A3 wt Allele Synonyms
SLC26A3 wt Allele, CLD, DRA, Solute Carrier Family 26, Member 3 wt Allele
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