Assay Details
Target Gene Details
Entrez Gene ID: | 116085 |
Gene Name: | solute carrier family 22 member 12 |
Gene Aliases: |
OAT4L, RST, URAT1 |
Location: |
Chr.11:64590810-64603250 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC22A12 | NM_001276326.1 | 10 | 2522 | NP_001263255.1 |
| NM_001276327.1 | 8 | 2300 | NP_001263256.1 | |
| NM_144585.3 | 10 | 2624 | NP_653186.2 | |
| NM_153378.2 | 10 | 2358 | NP_700357.1 | |
| XM_006718430.3 | 9 | 2305 | XP_006718493.1 | |
| XM_006718431.3 | 10 | 2191 | XP_006718494.1 | |
| AB050269.1 | 10 | 2621 | BAB68364.1 | |
| AB071863.1 | 10 | 2024 | BAB96750.1 | |
| AK055737.1 | 10 | 1940 | ||
| AK122599.1 | 10 | 2178 | ||
| AY358183.1 | 8 | 1833 | AAQ88550.1 | |
| BC026291.1 | ||||
| BC053348.1 | 10 | 2167 | AAH53348.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv528506 | Chr.11:64577976 - 64933558 on Build GRCh38 | Loss |
|
| esv2422214 | Chr.11:64545019 - 64715946 on Build GRCh38 | Deletion |
|
| dgv1965n54 | Chr.11:64566642 - 64806117 on Build GRCh38 | Loss |
|
| nsv832188 | Chr.11:64547896 - 64717737 on Build GRCh38 | Gain |
|
| nsv555197 | Chr.11:64596819 - 64608835 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs150284736] 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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Genomic Map