Profil protéine

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.

Alternative names and synonyms associated with Monocarboxylate Transporter 8 (MCT8)

• solute carrier family 16 member 2 (SLC16A2) anticorps
• solute carrier family 16 (monocarboxylic acid transporters), member 2 (Slc16a2) anticorps
• solute carrier family 16 member 2 (Slc16a2) anticorps

• AHDS anticorps
• AW105741 anticorps
• DXS128 anticorps
• DXS128E anticorps
• MCT 7 anticorps
• Afficher tous les alias de synonymes
• MCT7 anticorps
• Mct8 anticorps
• MCT 8 anticorps
• MRX22 anticorps
• XPCT anticorps

Protein level used designations for MCT8

monocarboxylate transporter 8 , MCT 8 , Monocarboxylate transporter 8 (MCT 8) (X-linked PEST-containing transporter) , X-linked PEST-containing transporter , solute carrier family 16 member 2 , monocarboxylate transporter 7 , solute carrier family 16 (monocarboxylic acid transporters), member 2 , solute carrier family 16, member 2 (monocarboxylic acid transporter 8)