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. 2017 Dec 13;18(12):2708. doi: 10.3390/ijms18122708

Table 1.

Physiological properties of SLC39A/ Zrt- and Irt-like protein (ZIP) transporters.

Genes/Proteins Expression Subcellular Location Physiological Functions Genetic Mutation Study in Mice References
Slc39a1/ZIP1 Ubiquitous Plasma membrane Abnormal embryonic development Knockout (KO) [12]
Slc39a2/ZIP2 Liver, ovary, skin, dendritic cell Plasma membrane Abnormal embryonic development KO [15]
Slc39a3/ZIP3 Widely distributed Plasma membrane Abnormal embryonic and T-cell development KO [12]
Slc39a4/ZIP4 Small intestine, epidermis Plasma membrane Embryonic lethality KO [16,17]
Slc39a5/ZIP5 Small intestine, kidney, pancreas Plasma membrane Intestinal Zn excretion; pancreatic Zn accumulation KO [18]
Slc39a6/ZIP6 Widely distributed Plasma membrane Abnormal gonad formation and E-cadherin expression - [19,20]
Glial cell migration in Drosophila
Slc39a7/ZIP7 Widely distributed, colon, skin Endoplasmic reticulum (ER) and Golgi apparatus Impaired melanin synthesis, fibroblast growth factor receptor (FGFR) and Notch signaling in Drosophila KO [21,22,23]
Colon epithelial cell differentiation and proliferation in mouse
Skin dermis development
Slc39a8/ZIP8 Widely distributed Plasma membrane, lysosome Cdm mouse: Resistance to cadmium-induced testicular damage, embryonic lethality KO [24,25]
Slc39a9/ZIP9 Widely distributed Golgi apparatus Expressed in breast and prostate cancer cell lines - [26,27]
Apoptosis regulation
Slc39a10/ZIP10 Widely distributed, renal cell, carcinoma B cell Plasma membrane B cell development and function. KO [28,29,30]
Epidermal development
Breast cancer progression
Slc39a12/ZIP12 Brain, pulmonary vascular smooth muscle Plasma membrane Neuronal differentiation KO (Rat) [31]
Attenuation of pulmonary hypertension in a hypoxic atmosphere
Slc39a13/ZIP13 Hard and connective tissues Golgi apparatus, vesicles Growth retardation, abnormal hard and connective tissue development, and adipocyte browning KO [32,33]
Growth retardation and impaired G protein-coupled receptor (GPCR) signaling
Slc39a14/ZIP14 Widely distributed, liver, bone, and cartilage Plasma membrane, endosome Growth retardation, abnormal chondrocyte differentiation KO [34,35,36,37,38]
Adipokineuction
Impaired the phosphodiesterase (PDE) activity through GPCR-mediated cAMP-CREB signaling
Hypertrophic adiposity
Endotoxemia
Glucose metabolism
Impaired ER stress