Gene Gene information from NCBI Gene database.
Entrez ID 26266
Gene name Solute carrier family 13 member 4
Gene symbol SLC13A4
Synonyms (NCBI Gene)
NAS2SUT-1SUT1
Chromosome 7
Chromosome location 7q33
miRNA miRNA information provided by mirtarbase database.
39
miRTarBase ID miRNA Experiments Reference
MIRT017301 hsa-miR-335-5p Microarray 18185580
MIRT029042 hsa-miR-26b-5p Microarray 19088304
MIRT497552 hsa-miR-6815-5p PAR-CLIP 22291592
MIRT497551 hsa-miR-6865-5p PAR-CLIP 22291592
MIRT497550 hsa-miR-3614-5p PAR-CLIP 22291592
Transcription factors Transcription factors information provided by TRRUST V2 database.
3
Transcription factor Regulation Reference
KLF7 Unknown 23485456
SP1 Unknown 23485456
ZIC2 Unknown 23485456
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane TAS 10535998
GO:0006811 Process Monoatomic ion transport IEA
GO:0006814 Process Sodium ion transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604309 15827 ENSG00000164707
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UKG4
Protein name Solute carrier family 13 member 4 (Na(+)/sulfate cotransporter SUT-1) (NaS2)
Protein function Sodium:sulfate symporter that mediates sulfate reabsorption in the high endothelial venules (HEV).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00939 Na_sulph_symp 5 610 Sodium:sulfate symporter transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in placenta and testis with intermediate levels in brain and lower levels in heart, thymus and liver. {ECO:0000269|PubMed:10535998, ECO:0000269|PubMed:15607730}.
Sequence
Sequence length 626
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Sodium-coupled sulphate, di- and tri-carboxylate transporters
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AUTISM SPECTRUM DISORDER CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
JUVENILE IDIOPATHIC ARTHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Fibrosis, Liver Liver Fibrosis CTD_human_DG 25226513
★☆☆☆☆
Found in Text Mining only
Head and Neck Neoplasms Head and neck neoplasm Pubtator 34840533 Inhibit
★☆☆☆☆
Found in Text Mining only
Liver Cirrhosis Liver Cirrhosis CTD_human_DG 25226513
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Squamous Cell Carcinoma of Head and Neck Squamous cell carcinoma Pubtator 34840533 Associate
★☆☆☆☆
Found in Text Mining only