Target intelligence / Profile preview

Zinc transporter 2 (ZnT2)

Target
ZnT2
Molecular classification
Transporter, Ion channel (specifically, monoatomic cation transmembrane transporter), Solute carrier family (SLC30)
01

Overview

Zinc transporter 2 (ZnT2; SLC30A2) is a member of the solute carrier family 30 and is primarily expressed in specialized secretory cells such as mammary epithelial cells. It functions as a proton-coupled antiporter, transporting zinc into secretory vesicles, thus ensuring adequate zinc secretion into breast milk—a crucial mechanism for neonatal development. Mutations in SLC30A2 lead to reduced zinc transport and secretion, manifesting clinically as transient neonatal zinc deficiency (TNZD) in exclusively breastfed infants. ZnT2’s subcellular localization and function are tightly regulated, and mutations can impair zinc transport through dominant-negative effects, haploinsufficiency, or altered protein trafficking and stability. While not a direct drug target in therapeutics, its genetic and physiological significance makes it a biomarker for lactational failure and zinc-deficiency disorders.

Other names
SLC30A2Zinc transporter 2ZnT2Solute carrier family 30 member 2Proton-coupled zinc antiporter SLC30A2TNZDPP12488ZNT2Solute carrier family 30 (zinc transporter), member 2
02

Mechanism of action

For therapeutic context: restoration of zinc transporter activity (e.g., via supplementation); Modulation of zinc secretion into breast milk

03

Biological functions

Zinc secretion into milkVesicular zinc accumulation and export, regulating cytosolic and organellar zinc levelsCellular zinc homeostasis and protection from zinc cytotoxicityModulation of cell death processes, especially in the mammary gland
04

Disease associations

Transient neonatal zinc deficiency (TNZD)Zinc deficiencyEhlers-Danlos syndrome, spondylodysplastic type 3Potential dysfunction in lactation, breast epithelial cell integrity, and neonatal immune development
05

Safety considerations

Zinc deficiency in breastfed infants (potentially resulting in severe developmental consequences)Unintended consequences of genetic screening, variable penetrance in populationsNo safety concerns for drugs, since no direct drugs exist for ZnT2 modulation
06

Biomarkers

Reduced milk zinc concentrationMutations in SLC30A2 (e.g., H54R, G87R, T288S, W152R, S296L)Clinical features of TNZD in breastfed infants

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