Genomic Map
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Target Gene Details
Entrez Gene ID: | 6304 |
Gene Name: | SATB homeobox 1 |
Gene Aliases: |
- |
Location: |
Chr.3:18345388-18445588 on Build GRCh38 |
Assay Gene Location: | Within Exon 17 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SATB1 | NM_001131010.3 | 11 | 4557 | NP_001124482.1 |
| NM_001195470.2 | 12 | 6155 | NP_001182399.1 | |
| NM_001322871.1 | 12 | 4701 | NP_001309800.1 | |
| NM_001322872.1 | 12 | 4605 | NP_001309801.1 | |
| NM_001322873.1 | 11 | 4605 | NP_001309802.1 | |
| NM_001322874.1 | 11 | 4419 | NP_001309803.1 | |
| NM_001322875.1 | 11 | 4417 | NP_001309804.1 | |
| NM_001322876.1 | 10 | 4370 | NP_001309805.1 | |
| NM_002971.5 | 11 | 6059 | NP_002962.1 | |
| AK124253.1 | 1 | 387 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv460455 | Chr.3:18344240 - 18386958 on Build GRCh38 | Loss |
 SATB1
|
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Additional Information:
For this assay, SNP(s) [rs68076437] 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: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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