Genomic Map
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Target Gene Details
Entrez Gene ID: | 9356 |
Gene Name: | solute carrier family 22 member 6 |
Gene Aliases: |
HOAT1, OAT1, PAHT, ROAT1 |
Location: |
Chr.11:62976597-62985023 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC22A6 | NM_004790.4 | 1 | 169 | NP_004781.2 |
| NM_153276.2 | 1 | 169 | NP_695008.1 | |
| NM_153277.2 | 1 | 169 | NP_695009.1 | |
| NM_153278.2 | 1 | 169 | NP_695010.1 | |
| XM_017018562.1 | 1 | 117 | XP_016874051.1 | |
| AB009697.1 | 1 | 103 | BAA75072.1 | |
| AB009698.1 | 1 | 100 | BAA75073.1 | |
| AF057039.2 | 1 | 80 | AAC70004.1 | |
| AF104038.1 | 1 | 81 | AAD10052.1 | |
| AF124373.1 | 1 | 93 | AAD55356.1 | |
| AK055764.1 | 1 | 145 | ||
| AK091879.1 | 1 | 113 | ||
| AK298374.1 | ||||
| BC033682.1 | 1 | 129 | AAH33682.1 | |
| DA628191.1 | 1 | 148 | ||
| DA629600.1 | 1 | 169 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv34011 | Chr.11:62885307 - 63226230 on Build GRCh38 | Loss |
 CHRM1
SLC22A24
SLC3A2
SLC22A25
SLC22A8
SLC22A6
|
| dgv204e214 | Chr.11:62950243 - 63024049 on Build GRCh38 | Gain |
SLC22A8
SLC22A6
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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