Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64078
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 28 member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC28A3
Synonyms (NCBI Gene) Gene synonyms aliases
CNT3
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q21.32-q21.33
Summary Summary of gene provided in NCBI Entrez Gene.
Nucleoside transporters, such as SLC28A3, regulate multiple cellular processes, including neurotransmission, vascular tone, adenosine concentration in the vicinity of cell surface receptors, and transport and metabolism of nucleoside drugs. SLC28A3 shows
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs885004 G>A Drug-response Intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1358135 hsa-miR-1226 CLIP-seq
MIRT1358136 hsa-miR-1246 CLIP-seq
MIRT1358137 hsa-miR-1290 CLIP-seq
MIRT1358138 hsa-miR-29a CLIP-seq
MIRT1358139 hsa-miR-29b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005337 Function Nucleoside transmembrane transporter activity IBA 21873635
GO:0005345 Function Purine nucleobase transmembrane transporter activity NAS 22492015
GO:0005415 Function Nucleoside:sodium symporter activity IBA 21873635
GO:0005415 Function Nucleoside:sodium symporter activity TAS
GO:0005789 Component Endoplasmic reticulum membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608269 16484 ENSG00000197506
Protein
UniProt ID Q9HAS3
Protein name Solute carrier family 28 member 3 (Concentrative Na(+)-nucleoside cotransporter 3) (CNT 3) (hCNT3)
Protein function Sodium-dependent, pyrimidine- and purine-selective (PubMed:11032837, PubMed:15861042, PubMed:16446384, PubMed:17140564, PubMed:21998139). Involved in the homeostasis of endogenous nucleosides (PubMed:11032837, PubMed:15861042). Exhibits the tran
PDB 6KSW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01773 Nucleos_tra2_N 205 277 Na+ dependent nucleoside transporter N-terminus Family
PF07670 Gate 285 385 Nucleoside recognition Domain
PF07662 Nucleos_tra2_C 388 612 Na+ dependent nucleoside transporter C-terminus Family
Tissue specificity TISSUE SPECIFICITY: Expressed in pancreas, bone marrow, trachea, mammary gland, liver, prostate, and regions of intestine, brain, lung, placenta, testis, kidney, and heart. {ECO:0000269|PubMed:11032837}.
Sequence
MELRSTAAPRAEGYSNVGFQNEENFLENENTSGNNSIRSRAVQSREHTNTKQDEEQVTVE
QDSPRNREHMEDDDEEMQQKGCLERRYDTVCGFCRKHKTTLRHIIWGILLAGYLVMVISA
CVLNFHRALPLFVITVAAIFFVVWDHLMAKYEHRIDEMLSPGRRLLNSHWFWLKWVIWSS
LVLAVIFWLAFDTAKLGQQQLVSFGGLIMYIVLLFLFSKYPTRVYWRPVLWGIGLQFLLG
LLILRTDPGFIAFDWLGRQVQTFLEYTDAGASFVFGE
KYKDHFFAFKVLPIVVFFSTVMS
MLYYLGLMQWIIRKVGWIMLVTTGSSPIESVVASGNIFVGQTESPLLVRPYLPYITKSEL
HAIMTAGFSTIAGSVLGAYISFGVP
SSHLLTASVMSAPASLAAAKLFWPETEKPKITLKN
AMKMESGDSGNLLEAATQGASSSISLVANIAVNLIAFLALLSFMNSALSWFGNMFDYPQL
SFELICSYIFMPFSFMMGVEWQDSFMVARLIGYKTFFNEFVAYEHLSKWIHLRKEGGPKF
VNGVQQYISIRSEIIATYALCGFANIGSLGIVIGGLTSMAPSRKRDIASGAVRALIAGTV
ACFMTACIAGIL
SSTPVDINCHHVLENAFNSTFPGNTTKVIACCQSLLSSTVAKGPGEVI
PGGNHSLYSLKGCCTLLNPSTFNCNGISNTF
Sequence length 691
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Androgenetic Alopecia Androgenetic Alopecia GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Alzheimer disease Alzheimer disease GWAS
Colorectal Cancer Colorectal Cancer In summary, our data strongly demonstrated that upregulation of GRB7 conferred MEKi resistance in CRC cells with KRAS mutations by mediating RTK signaling through the recruitment of PLK1. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Anemia Associate 23195617
Carcinoma Non Small Cell Lung Associate 22173087
Cardiomyopathies Associate 30351207
Cardiotoxicity Associate 33900042, 35110416
Drug Related Side Effects and Adverse Reactions Associate 30927276, 36952646
Hemorrhage Associate 36952646
Leukemia Lymphocytic Chronic B Cell Associate 12411296, 30778771
Neoplasms Associate 24300978, 36621142
Neurologic Manifestations Associate 36952646
Neutropenia Associate 30927276