Genomic Map
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Target Gene Details
Entrez Gene ID: | 6519 |
Gene Name: | solute carrier family 3 member 1 |
Gene Aliases: |
ATR1, CSNU1, D2H, NBAT, RBAT |
Location: |
Chr.2:44275458-44320824 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC3A1 | NM_000341.3 | NP_000332.2 | ||
| XM_011533047.2 | XP_011531349.1 | |||
| AB033549.1 | BAB16841.1 | |||
| AK091932.1 | ||||
| AK223146.1 | BAD96866.1 | |||
| AK289636.1 | ||||
| AK309145.1 | ||||
| AK313157.1 | ||||
| BC022386.1 | AAH22386.1 | |||
| BC093624.1 | AAH93624.1 | |||
| BC093626.1 | AAH93626.1 | |||
| DQ023513.1 | AAY89644.1 | |||
| DQ023515.1 | AAY89646.1 | |||
| DQ023516.1 | AAY89647.1 | |||
| DQ023517.1 | AAY89648.1 | |||
| KU178335.1 | ||||
| KU178336.1 | ||||
| L11696.1 | AAA81778.1 | |||
| M95548.1 | AAA35500.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv3798n100 | Chr.2:44279994 - 44404126 on Build GRCh38 | Loss |
 CAMKMT
PREPL
SLC3A1
|
| dgv6837n54 | Chr.2:44278046 - 44351759 on Build GRCh38 | Loss |
PREPL
SLC3A1
|
| esv3583768 | Chr.2:44279853 - 44284604 on Build GRCh38 | Loss |
SLC3A1
|
| nsv1006405 | Chr.2:44013164 - 44709137 on Build GRCh38 | Loss |
CAMKMT
PREPL
SLC3A1
PPM1B
|
| nsv1011655 | Chr.2:44278899 - 44344334 on Build GRCh38 | Loss |
PREPL
SLC3A1
|
| nsv457196 | Chr.2:44276990 - 44339733 on Build GRCh38 | Gain |
PREPL
SLC3A1
|
| nsv521399 | Chr.2:44280074 - 44317775 on Build GRCh38 | Loss |
PREPL
SLC3A1
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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