Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8170
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 14 member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC14A2
Synonyms (NCBI Gene) Gene synonyms aliases
HUT2, UT-A2, UT2, UTA, UTR, hUT-A6
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the urea transporter family. In mammalian cells, urea is the chief end product of nitrogen catabolism, and plays an important role in the urinary concentration mechanism. This protein is expressed in the inner m
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1352598 hsa-miR-106a CLIP-seq
MIRT1352599 hsa-miR-106b CLIP-seq
MIRT1352600 hsa-miR-1193 CLIP-seq
MIRT1352601 hsa-miR-1234 CLIP-seq
MIRT1352602 hsa-miR-1254 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane TAS
GO:0015204 Function Urea transmembrane transporter activity IEA
GO:0015840 Process Urea transport TAS 8647271
GO:0016020 Component Membrane TAS 8647271
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601611 10919 ENSG00000132874
Protein
UniProt ID Q15849
Protein name Urea transporter 2 (Solute carrier family 14 member 2) (Urea transporter, kidney)
Protein function [Isoform 1]: Mediates the transport of urea driven by a concentration gradient across the cell membrane of the renal inner medullary collecting duct which is critical to the urinary concentrating mechanism. {ECO:0000269|PubMed:11502588, ECO:0000
PDB 8BLO , 8XD7 , 8XD9 , 8XDA , 8XDB , 8XDC , 8XDD , 8XDE
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03253 UT 119 414 Urea transporter Family
PF03253 UT 581 876 Urea transporter Family
Tissue specificity TISSUE SPECIFICITY: [Isoform 1]: Epressed in the inner medulla of the kidney (at protein level). {ECO:0000269|PubMed:11502588}.; TISSUE SPECIFICITY: [Isoform 2]: Expressed in the kidney. {ECO:0000269|PubMed:8647271}.
Sequence
MSDPHSSPLLPEPLSSRYKLYEAEFTSPSWPSTSPDTHPALPLLEMPEEKDLRSSNEDSH
IVKIEKLNERSKRKDDGVAHRDSAGQRCICLSKAVGYLTGDMKEYRIWLKDKHLALQFID
WVLRGTAQVMFINNPLSGLIIFIGLLIQNPWWTITGGLGTVVSTLTALALGQDRSAIASG
LHGYNGMLVGLLMAVFSEKLDYYWWLLFPVTFTAMSCPVLSSALNSIFSKWDLPVFTLPF
NIAVTLYLAATGHYNLFFPTTLVEPVSSVPNITWTEMEMPLLLQAIPVGVGQVYGCDNPW
TGGVFLVALFISSPLICLHAAIGSIVGLLAALSVATPFETIYTGLWSYNCVLSCIAIGGM
FYALTWQTHLLALICALFCAYMEAAISNIMSVVGVPPGTWAFCLATIIFLLLTT
NNPAIF
RLPLSKVTYPEANRIYYLTVKSGEEEKAPSGGGGEHPPTAGPKVEEGSEAVLSKHRSVFH
IEWSSIRRRSKVFGKGEHQERQNKDPFPYRYRKPTVELLDLDTMEESSEIKVETNISKTS
WIRSSMAASGKRVSKALSYITGEMKECGEGLKDKSPVFQFFDWVLRGTSQVMFVNNPLSG
ILIILGLFIQNPWWAISGCLGTIMSTLTALILSQDKSAIAAGFHGYNGVLVGLLMAVFSD
KGDYYWWLLLPVIIMSMSCPILSSALGTIFSKWDLPVFTLPFNITVTLYLAATGHYNLFF
PTTLLQPASAMPNITWSEVQVPLLLRAIPVGIGQVYGCDNPWTGGIFLIALFISSPLICL
HAAIGSTMGMLAALTIATPFDSIYFGLCGFNSTLACIAIGGMFYVITWQTHLLAIACALF
AAYLGAALANMLSVFGLPPCTWPFCLSALTFLLLTT
NNPAIYKLPLSKVTYPEANRIYYL
SQERNRRASIITKYQAYDVS
Sequence length 920
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Transport of bile salts and organic acids, metal ions and amine compounds
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Follicular lymphoma Follicular lymphoma GWAS
Breast cancer Breast cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Gout Gout GWAS
Takayasu Arteritis Takayasu Arteritis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 34887858
Cardiovascular Diseases Associate 27981573
Drug Related Side Effects and Adverse Reactions Associate 27981573
Kidney Diseases Associate 26776194