Assay Details
Target Gene Details
Entrez Gene ID: | 6581 |
Gene Name: | solute carrier family 22 member 3 |
Gene Aliases: |
EMT, EMTH, OCT3 |
Location: |
Chr.6:160348373-160454982 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC22A3 | NM_021977.3 | NP_068812.1 | ||
XM_005267106.4 | XP_005267163.1 | |||
XM_005267107.3 | XP_005267164.1 | |||
XM_011536076.2 | XP_011534378.1 | |||
XM_017011203.1 | XP_016866692.1 | |||
AJ001417.1 | CAA04751.1 | |||
AK314590.1 | ||||
BP320971.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv35098 | Chr.6:160001557 - 160649838 on Build GRCh38 | Gain |
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nsv818463 | Chr.6:160014537 - 160604515 on Build GRCh38 | Gain |
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esv3611428 | Chr.6:160167929 - 160379860 on Build GRCh38 | Gain |
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nsv1026543 | Chr.6:160306836 - 161585804 on Build GRCh38 | Gain |
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esv2759484 | Chr.6:159951212 - 160813633 on Build GRCh38 | Gain+Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs117565453] 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: |
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Panther Classification:
Gene Ontology Categories:
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