SLC22A10 (solute carrier family 22 member 10 (gene/pseudogene))

Gene
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
387775
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 22 member 10 (gene/pseudogene)
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC22A10
Synonyms (NCBI Gene) Gene synonyms aliases
OAT5, hOAT5
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.3
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
Show/Hide all(9)
miRTarBase ID miRNA Experiments Reference
MIRT2104818 hsa-miR-4282 CLIP-seq
MIRT2690933 hsa-miR-133a CLIP-seq
MIRT2690934 hsa-miR-133b CLIP-seq
MIRT2690935 hsa-miR-2113 CLIP-seq
MIRT2690936 hsa-miR-3908 CLIP-seq
Transcription factors
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
Show/Hide all(1)
Transcription factor Regulation Reference
HNF1A Activation 20829431
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
Show/Hide all(4)
GO ID Ontology Definition Evidence Reference
GO:0015711 Process Organic anion transport IBA 21873635
GO:0016021 Component Integral component of membrane IEA
GO:0022857 Function Transmembrane transporter activity IEA
GO:0055085 Process Transmembrane transport IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
607580 18057 ENSG00000184999
Protein
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
UniProt ID Q63ZE4
Protein name Solute carrier family 22 member 10 (Organic anion transporter 5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 102 → 527 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Detected in fetal and adult liver, and in adult kidney. {ECO:0000269|PubMed:11327718, ECO:0000269|PubMed:12372408}.
Sequence
Sequence length 541
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Transcription factors Gene ontology Other IDs Protein Associated diseases
Show/Hide Causal Diseases (5)
Causal
Disease term Disease name dbSNP ID References
Conotruncal defect Conotruncal defect rs1564752095, rs1379104498, rs1825112395, rs1825112515, rs1312980498, rs1341550325 24800985
Conotruncal heart defect CONOTRUNCAL HEART MALFORMATIONS (disorder) rs267606914, rs587777422 24800985
Glioblastoma Glioblastoma, Glioblastoma Multiforme rs121913500, rs886042842, rs1555138291, rs1558518449, rs1567176006, rs1558650888 30705370
Lung carcinoma Non-Small Cell Lung Carcinoma rs1805076, rs121909071, rs121913530, rs112445441, rs121913529, rs121913535, rs121913297, rs121913279, rs104886003, rs397516975, rs11554290, rs121913364, rs121913351, rs121913369, rs121913355
View all (44 more)		 30705370
Show/Hide Text Mining Associations (4)
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 35173266
Dementia Associate 35173266
Inflammation Associate 35173266
Nerve Degeneration Associate 35173266