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SLC22A12

The protein encoded by this gene is a urate transporter and urate-anion exchanger which regulates the level of urate in the blood. This protein is an integral membrane protein primarily found in kidney. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]
Full Name
solute carrier family 22 (organic anion/urate transporter), member 12
Function
Electroneutral antiporter that translocates urate across the apical membrane of proximal tubular cells in exchange for monovalent organic or inorganic anions (PubMed:12024214, PubMed:22194875, PubMed:35144162, PubMed:35462902).
Involved in renal reabsorption of urate and helps maintaining blood levels of uric acid (PubMed:12024214, PubMed:22194875).
Mediates urate uptake by an exchange with organic anions such as (S)-lactate and nicotinate, and inorganic anion Cl- (PubMed:12024214).
Other inorganic anions such as Br-, I- and NO3- may also act as counteranions that exchange for urate (PubMed:12024214).
Also mediates orotate tubular uptake coupled with nicotinate efflux and to a lesser extent with lactate efflux, therefore displaying a potential role in orotate renal reabsorption (PubMed:21350910).
Orotate transport is Cl--dependent (PubMed:21350910).
Biological Process
Biological Process cellular homeostasis1 PublicationNAS:UniProtKB
Biological Process cellular response to insulin stimulusIEA:Ensembl
Biological Process organic anion transportManual Assertion Based On ExperimentIBA:GO_Central
Biological Process renal urate salt excretionIEA:Ensembl
Biological Process response to xenobiotic stimulusManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process urate metabolic processManual Assertion Based On ExperimentIMP:BHF-UCL
Biological Process urate transportManual Assertion Based On ExperimentIDA:UniProtKB
Cellular Location
Apical cell membrane
Involvement in disease
Hypouricemia renal 1 (RHUC1):
A disorder characterized by impaired uric acid reabsorption at the apical membrane of proximal renal tubule cells, and high urinary urate excretion. Patients often appear asymptomatic, but may be subject to exercise-induced acute renal failure, chronic renal dysfunction and nephrolithiasis.
PTM
N-glycosylated.

Anti-SLC22A12 antibodies

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Target: SLC22A12
Host: Rabbit
Antibody Isotype: IgG
Specificity: Human
Clone: CBXS-1315
Application*: P
Target: SLC22A12
Host: Mouse
Specificity: Human
Clone: CBXS-4400
Application*: WB, IP, E
Target: SLC22A12
Host: Mouse
Antibody Isotype: IgG2a, κ
Specificity: Human
Clone: 2B5
Application*: WB, E
For Research Use Only. Not For Clinical Use.
(P): Predicted
* Abbreviations
IFImmunofluorescence
IHImmunohistochemistry
IPImmunoprecipitation
WBWestern Blot
EELISA
MMicroarray
CIChromatin Immunoprecipitation
FFlow Cytometry
FNFunction Assay
IDImmunodiffusion
RRadioimmunoassay
TCTissue Culture
GSGel Supershift
NNeutralization
BBlocking
AActivation
IInhibition
DDepletion
ESELISpot
DBDot Blot
MCMass Cytometry/CyTOF
CTCytotoxicity
SStimulation
AGAgonist
APApoptosis
IMImmunomicroscopy
BABioassay
CSCostimulation
EMElectron Microscopy
IEImmunoelectrophoresis
PAPeptide Array
ICImmunocytochemistry
PEPeptide ELISA
MDMeDIP
SHIn situ hybridization
IAEnzyme Immunoassay
SEsandwich ELISA
PLProximity Ligation Assay
ECELISA(Cap)
EDELISA(Det)
BIBioimaging
IOImmunoassay
LFLateral Flow Immunoassay
LALuminex Assay
CImmunohistochemistry-Frozen Sections
PImmunohistologyp-Paraffin Sections
ISIntracellular Staining for Flow Cytometry
MSElectrophoretic Mobility Shift Assay
RIRNA Binding Protein Immunoprecipitation (RIP)
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