Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81796
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier organic anion transporter family member 5A1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLCO5A1
Synonyms (NCBI Gene) Gene synonyms aliases
OATP-J, OATP-RP4, OATP5A1, OATPJ, OATPRP4, SLC21A15
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a 12 transmembrane domain protein that is a member of the solute carrier organic anion transporter superfamily. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT653404 hsa-miR-6849-3p HITS-CLIP 23824327
MIRT653403 hsa-miR-6892-3p HITS-CLIP 23824327
MIRT680449 hsa-miR-3183 HITS-CLIP 23824327
MIRT680448 hsa-miR-4723-3p HITS-CLIP 23824327
MIRT680447 hsa-miR-6769b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IDA 21278488
GO:0005886 Component Plasma membrane IEA
GO:0015347 Function Sodium-independent organic anion transmembrane transporter activity IBA
GO:0016020 Component Membrane IEA
GO:0016323 Component Basolateral plasma membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613543 19046 ENSG00000137571
Protein
UniProt ID Q9H2Y9
Protein name Solute carrier organic anion transporter family member 5A1 (Organic anion transporter polypeptide-related protein 4) (OATP-RP4) (OATPRP4) (Solute carrier family 21 member 15)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03137 OATP 129 734 Organic Anion Transporter Polypeptide (OATP) family Family
PF07648 Kazal_2 556 603 Kazal-type serine protease inhibitor domain Domain
Sequence
MDEGTGLQPGAGEQLEAPATAEAVQERCEPETLRSKSLPVLSSASCRPSLSPTSGDANPA
FGCVDSSGHQELKQGPNPLAPSPSAPSTSAGLGDCNHRVDLSKTFSVSSALAMLQERRCL
YVVLTDSRCFLVCMCFLTFIQALMVSGYLSSVITTIERRYSLKSSESGLLVSCFDIGNLV
VVVFVSYFGGRGRRPLWLAVGGLLIAFGAALFALPHFISPPYQIQELNASAPNDGLCQGG
NSTATLEPPACPKDSGGNNHWVYVALFICAQILIGMGSTPIYTLGPTYLDDNVKKENSSL
YLAIMYVMGALGPAVGYLLGGLLIGFYVDPRNPVHLDQNDPRFIGNWWSGFLLCAIAMFL
VIFPMFTFPKKLPPRHKKKKKKKFSVDAVSDDDVLKEKSNNSEQADKKVSSMGFGKDVRD
LPRAAVRILSNMTFLFVSLSYTAESAIVTAFITFIPKFIESQFGIPASNASIYTGVIIVP
SAGVGIVLGGYIIKKLKLGARESAKLAMICSGVSLLCFSTLFIVGCESINLGGINIPYTT
GPSLTMPHRNLTGSC
NVNCGCKIHEYEPVCGSDGITYFNPCLAGCVNSGNLSTGIRNYTE
CTC
VQSRQVITPPTVGQRSQLRVVIVKTYLNENGYAVSGKCKRTCNTLIPFLVFLFIVTF
ITACAQPSAIIVTLRSVEDEERPFALGMQFVLLRTLAYIPTPIYFGAVIDTTCMLWQQEC
GVQGSCWEYNVTSF
RFVYFGLAAGLKFVGFIFIFLAWYSIKYKEDGLQRRRQREFPLSTV
SERVGHPDNARTRSCPAFSTQGEFHEETGLQKGIQCAAQTYPGPFPEAISSSADPGLEES
PAALEPPS
Sequence length 848
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Attention Deficit Hyperactivity Disorder Attention deficit hyperactivity disorder N/A N/A GWAS
Cervical Cancer Cervical cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 21278488
Carcinoma Hepatocellular Associate 21383546
Carcinoma Renal Cell Associate 37304236
Colonic Neoplasms Stimulate 21383546
Glioblastoma Associate 35295612
Liver Neoplasms Associate 21383546
Neoplasms Stimulate 21383546
Neoplasms Associate 26949921, 33196683
Prostate Cancer Hereditary 7 Associate 33619025
Prostatic Neoplasms Associate 33619025