Assay Details
Target Gene Details
Entrez Gene ID: | 5002 |
Gene Name: | solute carrier family 22 member 18 |
Gene Aliases: |
BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1A |
Location: |
Chr.11:2899721-2925246 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC22A18 | NM_001315501.1 | NP_001302430.1 | ||
| NM_001315502.1 | NP_001302431.1 | |||
| NM_002555.5 | NP_002546.3 | |||
| NM_183233.2 | NP_899056.2 | |||
| XM_011520141.2 | XP_011518443.2 | |||
| XM_011520142.2 | XP_011518444.2 | |||
| AB012083.1 | BAA32779.1 | |||
| AF028738.1 | AAB82727.1 | |||
| AF030302.1 | AAC17492.1 | |||
| AF037064.1 | AAC04787.1 | |||
| AF059663.1 | AAC14725.1 | |||
| AF070479.1 | AAC23505.1 | |||
| AL521035.3 | ||||
| BC015571.2 | AAH15571.1 | |||
| BM561526.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv951292 | Chr.11:2792271 - 2927870 on Build GRCh38 | Deletion |
|
| esv2759795 | Chr.11:2767814 - 2942382 on Build GRCh38 | Gain |
|
| nsv469930 | Chr.11:2831299 - 2924715 on Build GRCh38 | Loss |
|
| nsv467658 | Chr.11:2902596 - 2924715 on Build GRCh38 | Loss |
|
| nsv832050 | Chr.11:2868540 - 2963987 on Build GRCh38 | Loss |
|
| nsv467657 | Chr.11:2879188 - 2916401 on Build GRCh38 | Loss |
|
More Information
Set Membership: |
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Genomic Map