Genomic Map
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Target Gene Details
Entrez Gene ID: | 6491 |
Gene Name: | SCL/TAL1 interrupting locus |
Gene Aliases: |
MCPH7, SIL |
Location: |
Chr.1:47250139-47314787 on Build GRCh38 |
Assay Gene Location: | Within Exon 18 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| STIL | NM_001048166.1 | 15 | 2886 | NP_001041631.1 |
| NM_001282936.1 | 16 | 3092 | NP_001269865.1 | |
| NM_001282937.1 | 16 | 3041 | NP_001269866.1 | |
| NM_001282938.1 | 17 | 2954 | NP_001269867.1 | |
| NM_001282939.1 | 17 | 2765 | NP_001269868.1 | |
| NM_003035.2 | 15 | 2883 | NP_003026.2 | |
| XM_006710834.3 | 16 | 2960 | XP_006710897.1 | |
| XM_011541991.2 | 16 | 3626 | XP_011540293.1 | |
| XM_011541992.2 | 16 | 3609 | XP_011540294.1 | |
| XM_011541994.2 | 15 | 2832 | XP_011540296.1 | |
| XM_011541996.2 | 16 | 2745 | XP_011540298.1 | |
| XM_011541998.2 | 16 | 2691 | XP_011540300.1 | |
| XM_011542001.2 | 15 | 2886 | XP_011540303.1 | |
| XM_017002123.1 | 16 | 2742 | XP_016857612.1 | |
| XM_017002124.1 | 11 | 2162 | XP_016857613.1 | |
| XM_017002125.1 | 15 | 2883 | XP_016857614.1 | |
| XM_017002126.1 | 15 | 2832 | XP_016857615.1 | |
| AK128406.1 | 5 | 3210 | ||
| AK307519.1 | 15 | 2848 | ||
| BC053615.1 | 17 | 2733 | AAH53615.1 | |
| BC126223.1 | 15 | 2959 | ||
| BC144089.1 | 15 | 2908 | ||
| CR749851.1 | 15 | 2862 | CAH18699.1 | |
| M74558.1 | 16 | 3108 | AAA60550.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv822531 | Chr.1:47248220 - 47264411 on Build GRCh38 | Gain |
 STIL
|
| nsv1160846 | Chr.1:47249998 - 47266706 on Build GRCh38 | Duplication |
STIL
|
| nsv441692 | Chr.1:47247989 - 47263416 on Build GRCh38 | Gain |
STIL
|
| esv3578138 | Chr.1:47247976 - 47263403 on Build GRCh38 | Gain |
STIL
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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