Genomic Map
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Target Gene Details
Entrez Gene ID: | 9733 |
Gene Name: | squamous cell carcinoma antigen recognized by T-cells 3 |
Gene Aliases: |
DSAP1, P100, RP11-13G14, TIP110, p110, p110(nrb) |
Location: |
Chr.12:108522214-108561402 on Build GRCh38 |
Assay Gene Location: | Within Intron 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SART3 | NM_014706.3 | NP_055521.1 | ||
| XM_005269241.4 | XP_005269298.1 | |||
| XM_011539026.2 | XP_011537328.1 | |||
| AB020880.1 | BAA78384.1 | |||
| AF387506.1 | AAK69347.1 | |||
| AK225174.1 | ||||
| AK290209.1 | ||||
| AK299250.1 | ||||
| AK302332.1 | ||||
| AK304834.1 | ||||
| BC093784.1 | AAH93784.1 | |||
| BC111983.1 | AAI11984.1 | |||
| BC143253.1 | ||||
| CN349201.1 | ||||
| CR933631.1 | ||||
| D63879.1 | BAA09929.1 |
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Additional Information:
For this assay, SNP(s) [rs145444864] 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
Intronic
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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