Protein detail

NPT2A

Sodium-dependent phosphate transport protein 2A (Sodium-phosphate transport protein 2A) (Na(+)-dependent phosphate cotransporter 2A) (NaPi-3) (Sodium/phosphate cotransporter 2A) (Na(+)/Pi cotransporter 2A) (NaPi-2a) (Solute carrier family 34 member 1)

Entry name
NPT2A
UniProt ID
EVMP confidence score
0.50
Supporting publications (n)
1
Transmembrane count
8
Protein classification
Disease related genesHuman disease related genesMetabolic proteinsPlasma proteinsPotential drug targetsPredicted intracellular proteinsPredicted membrane proteinsTransporters
EVMP confidence score

Annotation confidence score; open for threshold definitions.

Extremely high >= 0.85High >= 0.70Medium >= 0.55Low >= 0.40
Basic Information13
Protein Names
Sodium-dependent phosphate transport protein 2A (Sodium-phosphate transport protein 2A) (Na(+)-dependent phosphate cotransporter 2A) (NaPi-3) (Sodium/phosphate cotransporter 2A) (Na(+)/Pi cotransporter 2A) (NaPi-2a) (Solute carrier family 34 member 1)
Protein Class (8)
Disease related genesHuman disease related genesMetabolic proteinsPlasma proteinsPotential drug targetsPredicted intracellular proteinsPredicted membrane proteinsTransporters
Protein Function (8)
  • Human disease related genes:Urinary system diseases:Kidney diseases
  • Predicted intracellular proteins
  • Human disease related genes:Congenital disorders of metabolism:Other congenital disorders of metabolism
  • Human disease related genes:Musculoskeletal diseases:Skeletal diseases
  • Potential drug targets
  • Transporters:Electrochemical Potential-driven transporters
  • Disease related genes
  • Human disease related genes:Congenital disorders of metabolism:Congenital disorders of amino acid metabolism
Transmembrane
104..125; Helical; Name=M1; 146..163; Helical; Name=M2; 166..185; Helical; Name=M3; 348..370; Helical; Name=M4; 413..436; Helical; Name=M5; 467..487; Helical; Name=M6; 514..534; Helical; Name=M7; 540..561; Helical; Name=M8
Transmembrane Count
8
Entrez Gene Symbol
Gene Synonym (5)
NAPI-3NPT2NPTIIaSLC11SLC17A2
Gene Description
Solute carrier family 34 member 1
Chromosome
5
Position
177379235-177398848
Supporting publications (n)
1
EVMP confidence score
0.50
Fluorescence & Localization3
Tissue SpecificbreastCell SpecificBreast hormone-responsive cellsSingle-Nuclei Brain Specificcommitted oligodendrocyte precursor
Function & Pathway7
Protein Function (8)
  • Human disease related genes:Urinary system diseases:Kidney diseases
  • Predicted intracellular proteins
  • Human disease related genes:Congenital disorders of metabolism:Other congenital disorders of metabolism
  • Human disease related genes:Musculoskeletal diseases:Skeletal diseases
  • Potential drug targets
  • Transporters:Electrochemical Potential-driven transporters
  • Disease related genes
  • Human disease related genes:Congenital disorders of metabolism:Congenital disorders of amino acid metabolism
Mediation Categories (3)
Clinical-translation mediationFusion and delivery mediationMetabolism mediation
Relations & Evidence22

Ligand-Receptor Signaling (21)

21 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
receptorreceptorOmniPathNoYesNoNoNo
intracellularintracellularComPPINoNoNoNoNo
intracellularintracellularGO_IntercellNoNoNoNoNo
intracellularintracellularOmniPathNoNoNoNoNo
transportertransporterSurfaceomeNoYesNoNoNo
solute_carriertransporterAlmen2009NoYesNoNoNo
slc34transporterSurfaceomeNoYesNoNoNo
slctransporterSurfaceomeNoYesNoNoNo
transportertransporterOmniPathNoYesNoNoNo
transmembranetransmembraneUniProt_locationNoNoNoNoNo
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Isolation & Detection Technology (1)

1 record.

EV Isolation MethodDetection MethodNumber of ReferencesReferences
Protein Organic Solvent PrecipitationMass Spectrometry132384937
Sequence, Structure & Domains7

Sequences

Length
639
Mass
68,937
Sequence
MLSYGERLGSPAVSPLPVRGGHVMRGTAFAYVPSPQVLHRIPGTSAYAFPSLGPVALAEHTCPCGEVLERHEPLPAKLALEEEQKPESRLVPKLRQAGAMLLKVPLMLTFLYLFVCSLDMLSSAFQLAGGKVAGDIFKDNAILSNPVAGLVVGILVTVLVQSSSTSTSIIVSMVSSGLLEVSSAIPIIMGSNIGTSVTNTIVALMQAGDRTDFRRAFAGATVHDCFNWLSVLVLLPLEAATGYLHHITRLVVASFNIHGGRDAPDLLKIITEPFTKLIIQLDESVITSIATGDESLRNHSLIQIWCHPDSLQAPTSMSRAEANSSQTLGNATMEKCNHIFVDTGLPDLAVGLILLAGSLVLLCTCLILLVKMLNSLLKGQVAKVIQKVINTDFPAPFTWVTGYFAMVVGASMTFVVQSSSVFTSAITPLIGLGVISIERAYPLTLGSNIGTTTTAILAALASPREKLSSAFQIALCHFFFNISGILLWYPVPCTRLPIRMAKALGKRTAKYRWFAVLYLLVCFLLLPSLVFGISMAGWQVMVGVGTPFGALLAFVVLINVLQSRSPGHLPKWLQTWDFLPRWMHSLKPLDHLITRATLCCARPEPRSPPLPPRVFLEELPPATPSPRLALPAHHNATRL
Alternative Products
Event=Alternative splicing; Named isoforms=2; Name=1; IsoId=Q06495-1; Sequence=Displayed; Name=2; IsoId=Q06495-2; Sequence=VSP_042311
Alternative Sequence
313..639; APTSMSRAEANSSQTLGNATMEKCNHIFVDTGLPDLAVGLILLAGSLVLLCTCLILLVKMLNSLLKGQVAKVIQKVINTDFPAPFTWVTGYFAMVVGASMTFVVQSSSVFTSAITPLIGLGVISIERAYPLTLGSNIGTTTTAILAALASPREKLSSAFQIALCHFFFNISGILLWYPVPCTRLPIRMAKALGKRTAKYRWFAVLYLLVCFLLLPSLVFGISMAGWQVMVGVGTPFGALLAFVVLINVLQSRSPGHLPKWLQTWDFLPRWMHSLKPLDHLITRATLCCARPEPRSPPLPPRVFLEELPPATPSPRLALPAHHNATRL -> QNLEGREITHFDLRKKQAMEDSSVPHCP (in isoform 2)

Domain & Motif Annotations

Protein Families
SLC34A transporter family
Sequence Similarities
Belongs to the SLC34A transporter family.
Clinical Relevance2
Disease Involvement (2)
Disease variantOsteoporosis
Supporting Publications1
PMIDTitleAbstract
32384937Alzheimer's disease progression characterized by alterations in the molecular profiles and biogenesis of brain extracellular vesicles.No abstract available