Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
144195
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 2 member 14
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC2A14
Synonyms (NCBI Gene) Gene synonyms aliases
GLUT14, SLC2A3P3
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p13.31
Summary Summary of gene provided in NCBI Entrez Gene.
Members of the glucose transporter (GLUT) family, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as glucose and fructose into all mammalian cells. GLUTs show tissue and cell-type specific expression (Wu and
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019157 hsa-miR-335-5p Microarray 18185580
MIRT025478 hsa-miR-34a-5p Proteomics 21566225
MIRT025478 hsa-miR-34a-5p Proteomics 21566225
MIRT027782 hsa-miR-98-5p Microarray 19088304
MIRT554224 hsa-miR-498 PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005355 Function Glucose transmembrane transporter activity IDA 28971850
GO:0005634 Component Nucleus HDA 21630459
GO:0005886 Component Plasma membrane IDA 27460888
GO:0005886 Component Plasma membrane TAS
GO:0007275 Process Multicellular organism development IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611039 18301 ENSG00000173262
Protein
UniProt ID Q8TDB8
Protein name Solute carrier family 2, facilitated glucose transporter member 14 (Glucose transporter type 14) (GLUT-14)
Protein function Hexose transporter that can mediate the transport of glucose and dehydroascorbate across the cell membrane.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 37 489 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in testis (PubMed:12504846, PubMed:27460888). Also expressed in small intestine, liver and kidney (PubMed:27460888). {ECO:0000269|PubMed:12504846, ECO:0000269|PubMed:27460888}.
Sequence
Sequence length 520
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Cellular hexose transport
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Intracranial aneurysm Intracranial Aneurysm rs1594095223 30823506
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)
25475535
Unknown
Disease term Disease name Evidence References Source
Intracranial Aneurysm Intracranial Aneurysm GWAS
Associations from Text Mining
Disease Name Relationship Type References
22q11 Deletion Syndrome Associate 27604636
Breast Neoplasms Associate 34525987
Heart Defects Congenital Associate 27604636
Insulin Resistance Associate 31996098
Psoriasis Associate 31996098