Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
114134
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 2 member 13
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC2A13
Synonyms (NCBI Gene) Gene synonyms aliases
HMIT
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019106 hsa-miR-335-5p Microarray 18185580
MIRT496282 hsa-miR-1910-3p PAR-CLIP 22291592
MIRT496281 hsa-miR-6511a-5p PAR-CLIP 22291592
MIRT496280 hsa-miR-6808-5p PAR-CLIP 22291592
MIRT496279 hsa-miR-6893-5p PAR-CLIP 22291592
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002020 Function Protease binding IPI 26094765
GO:0002020 Function Protease binding ISS 26094765
GO:0005365 Function Myo-inositol transmembrane transporter activity ISS
GO:0005366 Function Myo-inositol:proton symporter activity IBA 21873635
GO:0005366 Function Myo-inositol:proton symporter activity IDA 11500374
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611036 15956 ENSG00000151229
Protein
UniProt ID Q96QE2
Protein name Proton myo-inositol cotransporter (H(+)-myo-inositol cotransporter) (Hmit) (H(+)-myo-inositol symporter) (Solute carrier family 2 member 13)
Protein function H(+)-myo-inositol cotransporter (PubMed:11500374). Can also transport related stereoisomers (PubMed:11500374).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 84 425 Sugar (and other) transporter Family
PF00083 Sugar_tr 497 609 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in the brain. {ECO:0000269|PubMed:11500374}.
Sequence
Sequence length 648
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Inositol transporters
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)
19915576, 22451204, 22438815, 28011712, 24842889
Unknown
Disease term Disease name Evidence References Source
Leprosy Leprosy 25642632 ClinVar, GWAS
Insomnia Insomnia GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Ulcerative colitis Ulcerative colitis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Dental Plaque Associate 29482039
Leukemia Myeloid Acute Associate 31918632
Pancreatic Neoplasms Associate 30972876
Parkinson Disease Associate 22763023, 33341150
Squamous Cell Carcinoma of Head and Neck Stimulate 37542344
Supranuclear Palsy Progressive Associate 33341150, 35384155, 39260141