Assay Details
Target Gene Details
Entrez Gene ID: | 197135 |
Gene Name: | PAT1 homolog 2 |
Gene Aliases: |
Pat1a, hPat1a |
Location: |
Chr.15:44665732-44711389 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PATL2 | XM_011521338.2 | XP_011519640.1 | ||
| XM_011521339.2 | XP_011519641.1 | |||
| XM_011521340.2 | XP_011519642.1 | |||
| XM_011521343.2 | XP_011519645.1 | |||
| XM_011521345.2 | XP_011519647.1 | |||
| AK130783.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1517 | Chr.15:44662336 - 44697647 on Build GRCh38 | Insertion |
|
| esv2760029 | Chr.15:44676670 - 45130644 on Build GRCh38 | Gain+Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs80036040] 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: |
|

Genomic Map