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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded protein

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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded proteinMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.

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Description

Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival

Collagenase 3 in this family are involved in the breakdown of extracellular matrix in normal physiological processes

mesangiocapillary glomerulonephritis

Two transcript variants encoding distinct isoforms have been identified

S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded proteinMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.

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