Protein detail

GTR9

Solute carrier family 2, facilitated glucose transporter member 9 (Glucose transporter type 9) (GLUT-9) (Urate transporter)

Protein symbol
GTR9
UniProt ID
EVMP score
0.25
Frequency
2
Transmembrane count
12
Protein classification
Disease related genesHuman disease related genesMetabolic proteinsPotential drug targetsPredicted membrane proteinsTransporters
Basic Information
Protein Names
Solute carrier family 2, facilitated glucose transporter member 9 (Glucose transporter type 9) (GLUT-9) (Urate transporter)
Protein Class
Disease related genesHuman disease related genesMetabolic proteinsPotential drug targetsPredicted membrane proteinsTransporters
Protein Function
  • Human disease related genes:Urinary system diseases:Kidney diseases
  • Potential drug targets
  • Transporters:Electrochemical Potential-driven transporters
  • Disease related genes
  • Human disease related genes:Musculoskeletal diseases:Other musculoskeletal diseases
Transmembrane
52..72; Helical; Name=1; 108..128; Helical; Name=2; 141..161; Helical; Name=3; 172..192; Helical; Name=4; 201..221; Helical; Name=5; 232..252; Helical; Name=6; 317..337; Helical; Name=7; 355..375; Helical; Name=8; 382..402; Helical; Name=9; 416..436; Helical; Name=10; 452..472; Helical; Name=11; 479..499; Helical; Name=12
Transmembrane Count
12
Entrez Gene Symbol
Gene Synonym
Glut9GLUTXURATv1
Gene Description
Solute carrier family 2 member 9
Chromosome
4
Position
9771153-10054936
Frequency
2
EVMP Score
0.25
Fluorescence & Localization
Tissue SpecificretinaCell SpecificCone photoreceptor cellsBlood Cell SpecificneutrophilBlood Lineage Specificgranulocytes
Function & Pathway
Relations & Evidence

Enzyme-Mediated Modification

0 records.

Ligand-Receptor Signaling

22 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
transmembranetransmembraneTopDBNoNoNoNoNo
transmembranetransmembraneLOCATENoNoNoNoNo
transmembranetransmembraneRamilowski_locationNoNoNoNoNo
transmembranetransmembraneOmniPathNoNoNoNoNo
plasma_membraneplasma_membraneUniProt_locationNoNoNoNoNo
basolateral_cell_membraneplasma_membraneUniProt_locationNoNoNoNoNo
apical_cell_membraneplasma_membraneUniProt_locationNoNoNoNoNo
plasma_membraneplasma_membraneOmniPathNoNoNoNoNo
cell_surfacecell_surfaceSurfaceomeNoNoNoNoNo
cell_surfacecell_surfaceOmniPathNoNoNoNoNo
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Regulatory Interaction Network

0 records.

Protein Complex Composition

0 records.

Isolation & Detection Technology

1 record.

EV Isolation MethodDetection MethodNumber of ReferencesReferences
Differential UltracentrifugationSize Exclusion ChromatographyImmunoaffinity CaptureWestern blotting140098346
Sequence, Structure & Domains

Sequences

Length
540
Mass
58,702
Sequence
MARKQNRNSKELGLVPLTDDTSHAGPPGPGRALLECDHLRSGVPGGRRRKDWSCSLLVASLAGAFGSSFLYGYNLSVVNAPTPYIKAFYNESWERRHGRPIDPDTLTLLWSVTVSIFAIGGLVGTLIVKMIGKVLGRKHTLLANNGFAISAALLMACSLQAGAFEMLIVGRFIMGIDGGVALSVLPMYLSEISPKEIRGSLGQVTAIFICIGVFTGQLLGLPELLGKESTWPYLFGVIVVPAVVQLLSLPFLPDSPRYLLLEKHNEARAVKAFQTFLGKADVSQEVEEVLAESRVQRSIRLVSVLELLRAPYVRWQVVTVIVTMACYQLCGLNAIWFYTNSIFGKAGIPPAKIPYVTLSTGGIETLAAVFSGLVIEHLGRRPLLIGGFGLMGLFFGTLTITLTLQDHAPWVPYLSIVGILAIIASFCSGPGGIPFILTGEFFQQSQRPAAFIIAGTVNWLSNFAVGLLFPFIQKSLDTYCFLVFATICITGAIYLYFVLPETKNRTYAEISQAFSKRNKAYPPEEKIDSAVTDGKINGRP
Alternative Products
Event=Alternative splicing; Named isoforms=2; Name=1; Synonyms=SLC2A9-L, SLC2A9a; IsoId=Q9NRM0-1; Sequence=Displayed; Name=2; Synonyms=GLUT9deltaN, SLC2A9-S, SLC2A9b; IsoId=Q9NRM0-2; Sequence=VSP_034860
Alternative Sequence
1..50; MARKQNRNSKELGLVPLTDDTSHAGPPGPGRALLECDHLRSGVPGGRRRK -> MKLSKKDRGEDEESDSAKKKL (in isoform 2)

3D Structural Models

3D Structure
Electron microscopy (4)

Domain & Motif Annotations

Region
1..31; Disordered; 519..540; Disordered
Protein Families
  • Major facilitator superfamily
  • Sugar transporter (TC 2.A.1.1) family
  • Glucose transporter subfamily
Sequence Similarities
Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. Glucose transporter subfamily.
Clinical Relevance
Disease Involvement
Disease variant