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S26A4 Polyclonal Antibody, 100ul Mammalian Expression The protein may play a

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S26A4 Polyclonal Antibody, 100ul Mammalian Expression The protein may play aMutations 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

The protein may play a role in the adhesive interactions of activated T and NK cells during the late phase of the immune response

Alternatively spliced transcript variants have been observed for CNOT2

May play a role in the trafficking of activated/effector T-lymphocytes to inflammatory sites and other aspects of activated T-lymphocyte physiology

2001 [PubMed 11689425])

The activity of the encoded protein is regulated by polo-like kinase 1

S26A4 Polyclonal Antibody, 100ul Mammalian Expression The protein may play aMutations 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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