Hs04052726_cn

• Gene Symbol: SLCO4A1
• Assay Reference Genome Location: Chr.20:62664635 on build GRCh38
• Cytoband: 20q13.33

Target Gene Details

• Entrez Gene ID: 28231
• Gene Name: solute carrier organic anion transporter family member 4A1
• Gene Aliases: OATP-E, OATP1, OATP4A1, OATPE, OATPRP1, POAT, SLC21A12
• Location: Chr.20:62642445-62690700 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLCO4A1	NM_016354.3			NP_057438.3
	XM_005260203.2			XP_005260260.1
	XM_011528792.2			XP_011527094.1
	XM_017027826.1			XP_016883315.1
	XM_017027827.1			XP_016883316.1
	AB031051.1			BAA89288.1
	AF104334.1			AAF15545.1
	AF187817.1			AAG43447.1
	AF205072.1			AAG42204.1
	AK023410.1			BAB14566.1
	BC015727.1			AAH15727.1

Target Gene Details

• Entrez Gene ID: 100127888
• Gene Name: SLCO4A1 antisense RNA 1
• Gene Aliases: -
• Location: Chr.20:62663027-62666621 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLCO4A1-AS1	NR_024470.1
	BC025345.1			AAH25345.1
	BU741282.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2422398	Chr.20:62207833 - 62674040 on Build GRCh38	Duplication	GATA5 LOC105369209 C20orf166-AS1 HRH3 MIR133A2 ADRM1 MIR4758 OSBPL2 RBBP8NL MIR1-1 LAMA5-AS1 MIR1-1HG CABLES2 RPS21 SLCO4A1-AS1 SLCO4A1 LAMA5
nsv586504	Chr.20:62658391 - 62688263 on Build GRCh38	Loss	SLCO4A1-AS1 SLCO4A1
nsv834026	Chr.20:62636291 - 62795287 on Build GRCh38	Loss	LOC107987285 NTSR1 SLCO4A1-AS1 SLCO4A1 LOC107985428 LINC00659
nsv586496	Chr.20:62332390 - 62812195 on Build GRCh38	Gain	LOC107987285 GATA5 C20orf166-AS1 MIR133A2 OGFR-AS1 MRGBP NTSR1 LOC107985428 MIR4758 RBBP8NL MIR1-1 LAMA5-AS1 MIR1-1HG CABLES2 RPS21 SLCO4A1-AS1 SLCO4A1 LAMA5 LINC00659 OGFR
nsv586503	Chr.20:62645662 - 62776055 on Build GRCh38	Gain	LOC107987285 NTSR1 SLCO4A1-AS1 SLCO4A1 LOC107985428 LINC00659
nsv953302	Chr.20:62345345 - 62831248 on Build GRCh38	Deletion	LOC107987285 GATA5 C20orf166-AS1 MIR133A2 OGFR-AS1 MRGBP NTSR1 LOC107985428 RBBP8NL MIR1-1 COL9A3 LAMA5-AS1 MIR1-1HG CABLES2 RPS21 SLCO4A1-AS1 SLCO4A1 LAMA5 LINC00659 OGFR
nsv428380	Chr.20:62632018 - 62935383 on Build GRCh38	Loss	LOC107987285 OGFR-AS1 MRGBP NTSR1 LOC107985428 DPH3P1 COL9A3 TCFL5 SLCO4A1-AS1 SLCO4A1 DIDO1 LINC00659 OGFR

More Information

Additional Information:

For this assay, SNP(s) [rs78526844] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

transporter

Gene Ontology Categories:

Process(es)

thyroid hormone metabolic process
sodium-independent organic anion transport
thyroid hormone transport

Function(s)

sodium-independent organic anion transmembrane transporter activity
thyroid hormone transmembrane transporter activity