Assay Details
Target Gene Details
Entrez Gene ID: | 151056 |
Gene Name: | phospholipase B1 |
Gene Aliases: |
PLB, PLB/LIP, hPLB |
Location: |
Chr.2:28488579-28644135 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PLB1 | NM_001170585.1 | NP_001164056.1 | ||
NM_153021.4 | NP_694566.4 | |||
XM_011532579.2 | XP_011530881.1 | |||
XM_011532581.2 | XP_011530883.1 | |||
XM_011532584.2 | XP_011530886.1 | |||
XM_011532588.2 | XP_011530890.1 | |||
XM_011532589.2 | XP_011530891.1 | |||
XM_011532590.2 | XP_011530892.1 | |||
XM_011532591.2 | XP_011530893.1 | |||
XM_011532593.2 | XP_011530895.1 | |||
XM_011532606.2 | XP_011530908.1 | |||
XM_011532607.2 | XP_011530909.1 | |||
XM_011532608.2 | XP_011530910.1 | |||
XM_017003432.1 | XP_016858921.1 | |||
XM_017003433.1 | XP_016858922.1 | |||
XM_017003434.1 | XP_016858923.1 | |||
BC150633.1 | ||||
BC153864.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv455985 | Chr.2:28513715 - 28546414 on Build GRCh38 | Gain | PLB1 |
dgv6745n54 | Chr.2:28513131 - 28546414 on Build GRCh38 | Gain | PLB1 |
More Information
Additional Information:
For this assay, SNP(s) [rs72792951] 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 Non-exonic DGV Variation |