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SLC5A6
Gene Name
solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Plasma Membrane
Integral Component Of Plasma Membrane
Vesicle Membrane
Membrane
Brush Border Membrane
Molecular Function
Sodium-dependent Multivitamin Transmembrane Transporter Activity
Biological Process
Vitamin Metabolic Process
Water-soluble Vitamin Metabolic Process
Biotin Metabolic Process
Transport
Sodium Ion Transport
Biotin Transport
Pantothenate Transmembrane Transport
Pantothenate Metabolic Process
Small Molecule Metabolic Process
Transmembrane Transport
Pathways
Metabolism of vitamins and cofactors
Defective CD320 causes methylmalonic aciduria
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
Defective BTD causes biotidinase deficiency
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
SLC-mediated transmembrane transport
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
Defective AMN causes hereditary megaloblastic anemia 1
Transport of vitamins, nucleosides, and related molecules
Defects in cobalamin (B12) metabolism
Defective GIF causes intrinsic factor deficiency
Vitamin B5 (pantothenate) metabolism
Defective HLCS causes multiple carboxylase deficiency
Defective MMAB causes methylmalonic aciduria type cblB
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Defective MMAA causes methylmalonic aciduria type cblA
Defective CUBN causes hereditary megaloblastic anemia 1
Defective MUT causes methylmalonic aciduria mut type
Metabolism of water-soluble vitamins and cofactors
Defects in biotin (Btn) metabolism
Defective TCN2 causes hereditary megaloblastic anemia
Biotin transport and metabolism
Defects in vitamin and cofactor metabolism
Drugs
Biotin
Lipoic Acid
Diseases
GWAS
Protein-protein Interactions
2 interactors:
ERBB2IP
GALNT6
Entrez ID
8884
HPRD ID
04934
Ensembl ID
ENSG00000138074
Uniprot IDs
Q9HD19
Q9Y289
PDB IDs
Enriched GO Terms of Interacting Partners
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Basal Protein Localization
Establishment Or Maintenance Of Epithelial Cell Apical/basal Polarity
Asymmetric Protein Localization
Establishment Or Maintenance Of Apical/basal Cell Polarity
Intermediate Filament Cytoskeleton Organization
Intermediate Filament-based Process
O-glycan Processing
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