General Information of the Ferroptosis Regulator (ID: REG10444)
Regulator Name Metal cation symporter ZIP14 (SLC39A14)
Synonyms
LIV-1 subfamily of ZIP zinc transporter 4; Solute carrier family 39 member 14; Zrt- and Irt-like protein 14
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Gene Name SLC39A14
Gene ID 23516
Regulator Type Protein coding
Uniprot ID Q15043
Sequence
MKLLLLHPAFQSCLLLTLLGLWRTTPEAHASSLGAPAISAASFLQDLIHRYGEGDSLTLQ
QLKALLNHLDVGVGRGNVTQHVQGHRNLSTCFSSGDLFTAHNFSEQSRIGSSELQEFCPT
ILQQLDSRACTSENQENEENEQTEEGRPSAVEVWGYGLLCVTVISLCSLLGASVVPFMKK
TFYKRLLLYFIALAIGTLYSNALFQLIPEAFGFNPLEDYYVSKSAVVFGGFYLFFFTEKI
LKILLKQKNEHHHGHSHYASESLPSKKDQEEGVMEKLQNGDLDHMIPQHCSSELDGKAPM
VDEKVIVGSLSVQDLQASQSACYWLKGVRYSDIGTLAWMITLSDGLHNFIDGLAIGASFT
VSVFQGISTSVAILCEEFPHELGDFVILLNAGMSIQQALFFNFLSACCCYLGLAFGILAG
SHFSANWIFALAGGMFLYISLADMFPEMNEVCQEDERKGSILIPFIIQNLGLLTGFTIMV
VLTMYSGQIQIG

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Family ZIP transporter family
Function
Electroneutral transporter of the plasma membrane mediating the cellular uptake of the divalent metal cations zinc, manganese and iron that are important for tissue homeostasis, metabolism, development and immunity. Functions as an energy-dependent symporter, transporting through the membranes an electroneutral complex composed of a divalent metal cation and two bicarbonate anions (By similarity). Beside these endogenous cellular substrates, can also import cadmium a non-essential metal which is cytotoxic and carcinogenic (By similarity). Controls the cellular uptake by the intestinal epithelium of systemic zinc, which is in turn required to maintain tight junctions and the intestinal permeability (By similarity). Modifies the activity of zinc-dependent phosphodiesterases, thereby indirectly regulating G protein-coupled receptor signaling pathways important for gluconeogenesis and chondrocyte differentiation (By similarity). Regulates insulin receptor signaling, glucose uptake, glycogen synthesis and gluconeogenesis in hepatocytes through the zinc-dependent intracellular catabolism of insulin. Through zinc cellular uptake also plays a role in the adaptation of cells to endoplasmic reticulum stress (By similarity). Major manganese transporter of the basolateral membrane of intestinal epithelial cells, it plays a central role in manganese systemic homeostasis through intestinal manganese uptake. Also involved in manganese extracellular uptake by cells of the blood-brain barrier. May also play a role in manganese and zinc homeostasis participating in their elimination from the blood through the hepatobiliary excretion (By similarity). Also functions in the extracellular uptake of free iron. May also function intracellularly and mediate the transport from endosomes to cytosol of iron endocytosed by transferrin. Plays a role in innate immunity by regulating the expression of cytokines by activated macrophages.

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HGNC ID
HGNC:20858
KEGG ID hsa:23516
Full List of the Ferroptosis Target of This Regulator and Corresponding Disease/Drug Response(s)
SLC39A14 can regulate the following target(s), and cause disease/drug response(s). You can browse detail information of target(s) or disease/drug response(s).
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Unspecific Target [Unspecific Target]
In total 1 item(s) under this target
Experiment 1 Reporting the Ferroptosis Target of This Regulator [1]
Responsed Disease Lung injury ICD-11: NB32
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model
MLE-12 cells Normal Mus musculus CVCL_3751
In Vivo Model
8- to 10-week-old male C57BL/6 mice were administered 2.5 ug/mL lipopolysaccharide (Escherichia coliserotype 0111: B4) via the trachea. After LPS administration for 6, 12, 24 and 48 h, the mice were euthanized and exsanguinated by cardiac puncture, and the lung tissue was removed for subsequent analysis.

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Response regulation The study identified three immune-mediated ferroptosis genes, namely, Cp, Slc7a11 and Slc39a14, which possibly regulated by neutrophils during the development of acute lung injury, and their pathways may be involved in anti-oxidative stress and anti-lipid metabolism.
Lung injury [ICD-11: NB32]
In total 1 item(s) under this disease
Experiment 1 Reporting the Ferroptosis-centered Disease Response [1]
Target Regulator Metal cation symporter ZIP14 (SLC39A14) Protein coding
Pathway Response Fatty acid metabolism hsa01212
Ferroptosis hsa04216
Cell Process Cell ferroptosis
In Vitro Model
MLE-12 cells Normal Mus musculus CVCL_3751
In Vivo Model
8- to 10-week-old male C57BL/6 mice were administered 2.5 ug/mL lipopolysaccharide (Escherichia coliserotype 0111: B4) via the trachea. After LPS administration for 6, 12, 24 and 48 h, the mice were euthanized and exsanguinated by cardiac puncture, and the lung tissue was removed for subsequent analysis.

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Response regulation The study identified three immune-mediated ferroptosis genes, namely, Cp, Slc7a11 and Slc39a14, which possibly regulated by neutrophils during the development of acute lung injury, and their pathways may be involved in anti-oxidative stress and anti-lipid metabolism.
References
Ref 1 Ferroptosis-related signature and immune infiltration characterization in acute lung injury/acute respiratory distress syndrome. Respir Res. 2023 Jun 10;24(1):154. doi: 10.1186/s12931-023-02429-y.