Assay Details
Target Gene Details
Entrez Gene ID: | 9651 |
Gene Name: | phospholipase C eta 2 |
Gene Aliases: |
PLC-L4, PLC-eta2, PLCL4, PLCeta2 |
Location: |
Chr.1:2412481-2505530 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PLCH2 | XM_011542455.2 | XP_011540757.1 | ||
XM_011542456.2 | XP_011540758.1 | |||
XM_017002870.1 | XP_016858359.1 | |||
XM_017002872.1 | XP_016858361.1 | |||
XM_017002873.1 | XP_016858362.1 | |||
XM_017002874.1 | XP_016858363.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv951557 | Chr.1:2266062 - 2564661 on Build GRCh38 | Deletion | LOC115110 HES5 MORN1 PLCH2 PANK4 SKI LOC100129534 RER1 TNFRSF14 PEX10 |
dgv50n54 | Chr.1:2401592 - 2518955 on Build GRCh38 | Loss | PLCH2 PANK4 RER1 PEX10 |
nsv470684 | Chr.1:2394570 - 2930923 on Build GRCh38 | Loss | LOC115110 HES5 PLCH2 PANK4 MMEL1 LOC100996583 TTC34 RER1 TNFRSF14 FAM213B PEX10 |
More Information
Additional Information:
For this assay, SNP(s) [rs80045357] 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 DGV Variation |