Target intelligence / Profile preview

Monocarboxylate transporter 10 (MCT10)

Target
MCT10
Molecular classification
Transporter, Monocarboxylate transporter family, Solute carrier (SLC) family, Major facilitator superfamily (MFS)
01

Overview

Monocarboxylate transporter 10 (MCT10), encoded by the SLC16A10 gene, is a membrane transporter belonging to the monocarboxylate transporter family and the major facilitator superfamily. It is primarily responsible for the sodium- and proton-independent transport of aromatic amino acids (phenylalanine, tyrosine, tryptophan) and has significant activity in facilitating both the uptake and efflux of thyroid hormones, especially triiodothyronine (T3) and thyroxine (T4), across cell membranes. Unlike MCT8, which is highly specific for thyroid hormone transport, MCT10 can also transport amino acids and may play a role in modulating intracellular thyroid hormone concentrations in various tissues, including neural and endocrine organs. Deficiencies or abnormalities in this transporter are linked to altered hormone availability, but no direct pathogenic mutations leading to monogenic disease have been conclusively established for MCT10. It is an active area of study for understanding hormone homeostasis and potential therapeutic manipulation.

Other names
SLC16A10Solute carrier family 16 member 10T-type amino acid transporter 1 (TAT1)Aromatic amino acid transporter 1
02

Mechanism of action

Facilitated diffusion (sodium- and proton-independent transport) of thyroid hormones and aromatic amino acids across the plasma membrane.

03

Biological functions

Transport of aromatic amino acids (phenylalanine, tyrosine, tryptophan)Transport of thyroid hormones (triiodothyronine T3, thyroxine T4)Regulation of intracellular thyroid hormone concentrationFacilitation of thyroid hormone uptake and efflux
04

Disease associations

Neurological disorders (as modifiers, e.g., in Allan-Herndon-Dudley syndrome, although not directly causative)Disorders related to thyroid hormone transport and metabolismPossible involvement in metabolic and endocrine disorders
05

Safety considerations

Loss or mutation of related transporter MCT8 leads to severe neurological deficits (Allan-Herndon-Dudley syndrome); however, for MCT10, direct disease associations and specific therapeutic safety concerns are not well established.Redundant or compensatory mechanisms due to expression of multiple thyroid hormone transporters may limit effectiveness of direct inhibition.
06

Interacting drugs

No clinically approved drugs specifically targeting MCT10 are established.

2 more in the full profile.

07

Biomarkers

Mutations or altered expression levels of SLC16A10/MCT10 may serve as tissue biomarkers for altered thyroid hormone or amino acid transport, though there are no established clinical biomarkers specific to MCT10.

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