Assay Details
Target Gene Details
Entrez Gene ID: | 219988 |
Gene Name: | PAT1 homolog 1, processing body mRNA decay factor |
Gene Aliases: |
Pat1b, hPat1b |
Location: |
Chr.11:59636716-59669040 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PATL1 | NM_152716.2 | 19 | 3931 | NP_689929.2 |
| XM_005273833.4 | 19 | 5053 | XP_005273890.1 | |
| XM_005273834.1 | 18 | 3843 | XP_005273891.1 | |
| XM_011544811.2 | 15 | 3266 | XP_011543113.1 | |
| XM_017017339.1 | 20 | 4007 | XP_016872828.1 | |
| AB065087.1 | 4 | 1830 | BAB93524.1 | |
| AK094193.1 | 16 | 3442 | BAC04305.1 | |
| AK127649.1 | 8 | 2373 | ||
| AL831992.2 | 19 | 3872 | CAD89916.1 | |
| BC065264.1 | 16 | 3425 | ||
| BC111047.1 | 17 | 3593 | AAI11048.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832172 | Chr.11:59628934 - 59663642 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76478883] 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: |
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Genomic Map