Genomic Map
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Target Gene Details
Entrez Gene ID: | 8848 |
Gene Name: | TSC22 domain family member 1 |
Gene Aliases: |
Ptg-2, TGFB1I4, TSC22 |
Location: |
Chr.13:44432143-44576565 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TSC22D1 | NM_001243799.1 | 1 | 415 | NP_001230728.1 |
| NM_183422.3 | 1 | 415 | NP_904358.2 | |
| XM_005266583.4 | 1 | 278 | XP_005266640.1 | |
| XM_017020810.1 | 1 | 278 | XP_016876299.1 | |
| XM_017020811.1 | 1 | 278 | XP_016876300.1 | |
| AB082525.1 | 1 | 415 | ||
| AK091854.1 | 1 | 106 | ||
| BC136475.1 | 1 | 185 | ||
| BC136482.1 | 1 | 185 |
Target Gene Details
Entrez Gene ID: | 641467 |
Gene Name: | TSC22D1 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.13:44575896-44580432 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TSC22D1-AS1 | NR_038381.1 | 1 | 256 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1124673 | Chr.13:44572864 - 44576164 on Build GRCh38 | Duplication |
 TSC22D1-AS1
TSC22D1
|
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Additional Information:
For this assay, SNP(s) [rs111570577] 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
|
Gene Ontology Categories:
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