SLC26A3 wt Allele

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). (NCI Thesaurus)

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SLC26A3 Gene

This gene plays a role in sulfate transport.

SLC25A6 wt Allele

Human SLC25A6 wild-type allele is located in the vicinity of both Xp22.32 and Yp11.3 and is approximately 6 kb in length. This…

SLC25A6 Gene

This gene plays a role in energy metabolism and nucleotide transport.

SLC25A5 wt Allele

Human SLC25A5 wild-type allele is located within Xq24-q26 and is approximately 3 kb in length. This allele, which encodes ADP/ATP translocase 2…

SLC25A5 Gene

This gene plays a regulatory role in the production and utilization of ATP.

SLC25A4 wt Allele

Human SLC25A4 wild-type allele is located in the vicinity of 4q35 and is approximately 4 kb in length. This allele, which encodes…