Gene Gene information from NCBI Gene database.
Entrez ID 55974
Gene name Solute carrier family 50 member 1
Gene symbol SLC50A1
Synonyms (NCBI Gene)
HsSWEET1RAG1AP1SCPSWEET1slv
Chromosome 1
Chromosome location 1q22
miRNA miRNA information provided by mirtarbase database.
225
miRTarBase ID miRNA Experiments Reference
MIRT004886 hsa-miR-124-3p Microarray 15685193
MIRT004886 hsa-miR-124-3p Microarray 18668037
MIRT043361 hsa-miR-331-3p CLASH 23622248
MIRT1365285 hsa-miR-1224-3p CLIP-seq
MIRT1365286 hsa-miR-1227 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IDA 21107422
GO:0005794 Component Golgi apparatus IEA
GO:0005886 Component Plasma membrane IDA 21107422
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613683 30657 ENSG00000169241
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BRV3
Protein name Sugar transporter SWEET1 (HsSWEET1) (RAG1-activating protein 1) (Solute carrier family 50 member 1) (Stromal cell protein)
Protein function Mediates sugar transport across membranes. May stimulate V(D)J recombination by the activation of RAG1.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03083 MtN3_slv 9 95 Sugar efflux transporter for intercellular exchange Family
PF03083 MtN3_slv 127 213 Sugar efflux transporter for intercellular exchange Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed with highest expression in oviduct, epididymis and intestine. {ECO:0000269|PubMed:21107422}.
Sequence
Sequence length 221
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.).
1
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
PARKINSON DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Neurodegenerative Diseases Associate 21348431
★☆☆☆☆
Found in Text Mining only