Assay Details
Target Gene Details
Entrez Gene ID: | 400961 |
Gene Name: | poly(A) binding protein interacting protein 2B |
Gene Aliases: |
- |
Location: |
Chr.2:71182738-71227110 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PAIP2B | NM_020459.1 | NP_065192.1 | ||
XM_005264310.3 | XP_005264367.1 | |||
XM_005264311.4 | XP_005264368.1 | |||
XM_011532842.2 | XP_011531144.1 | |||
XM_011532843.2 | XP_011531145.1 | |||
AB032981.1 | ||||
DA247526.1 | ||||
DA346299.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv508148 | Chr.2:71120178 - 71201982 on Build GRCh38 | Deletion | MPHOSPH10 MCEE PAIP2B |
nsv834256 | Chr.2:71029484 - 71202682 on Build GRCh38 | Gain | MPHOSPH10 OR7E91P MCEE PAIP2B NAGK OR7E62P |
More Information
Additional Information:
For this assay, SNP(s) [rs556133453] 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 |