Gene Gene information from NCBI Gene database.
Entrez ID 200010
Gene name Solute carrier family 5 member 9
Gene symbol SLC5A9
Synonyms (NCBI Gene)
SGLT4
Chromosome 1
Chromosome location 1p33
miRNA miRNA information provided by mirtarbase database.
15
miRTarBase ID miRNA Experiments Reference
MIRT1365845 hsa-miR-128 CLIP-seq
MIRT1365846 hsa-miR-1343 CLIP-seq
MIRT1365847 hsa-miR-1915 CLIP-seq
MIRT1365848 hsa-miR-1976 CLIP-seq
MIRT1365849 hsa-miR-3065-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005362 Function Low-affinity D-glucose:sodium symporter activity TAS
GO:0005402 Function Carbohydrate:monoatomic cation symporter activity IEA
GO:0005412 Function D-glucose:sodium symporter activity IBA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620216 22146 ENSG00000117834
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q2M3M2
Protein name Sodium/glucose cotransporter 4 (Na(+)/glucose cotransporter 4) (hSGLT4) (Solute carrier family 5 member 9)
Protein function Electrogenic Na(+)-coupled sugar symporter that may play a primary role in D-mannose and possibly D-fructose and D-glucose transport at the plasma membrane. Transporter activity is driven by a transmembrane Na(+) electrochemical gradient set by
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00474 SSF 67 496 Sodium:solute symporter family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the small intestine, kidney and liver. {ECO:0000269|PubMed:15607332}.
Sequence
Sequence length 681
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Cellular hexose transport
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SLC5A9-related disorder Benign; Likely benign ClinVar
★★☆☆☆
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
Colorectal Neoplasms Colorectal neoplasm Pubtator 23350875 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal Neoplasms BEFREE 31526853
★☆☆☆☆
Found in Text Mining only
Hypertension Hypertension Pubtator 40306283 Associate
★☆☆☆☆
Found in Text Mining only
Kidney Neoplasms Kidney neoplasm Pubtator 31526853 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31526853
★☆☆☆☆
Found in Text Mining only