SLC16A2

gene product
AHDS, DXS128, MCT7, MCT8, MRX22, XPCT
This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012]
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AntibodyRefsTypeAVIWBELICCIPIHCFC
Atlas Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
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NovoPro Bioscience Inc.
2 antibodies
Acris Antibodies GmbH
1 antibody
Proteintech Group
1 antibody
Novus Biologicals
3 antibodies
OriGene
2 antibodies
Biorbyt
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Affinity Biosciences
1 antibody
Bethyl Laboratories
1 antibody
antibodies-online
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Aviva Systems Biology
1 antibody
Invitrogen Antibodies
3 antibodies
Bioworld Technology, Inc
1 antibody
St John's Laboratory
2 antibodies
Abnova Corporation
2 antibodies
GeneTex
1 antibody
Abbkine Scientific Co.Ltd.
1 antibody
Abgent
1 antibody
EMD Millipore
1 antibody
Sigma-Aldrich
1 antibody
United States Biological
24 antibodies
MyBioSource
3 antibodies
Creative Diagnostics
1 antibody