Assay Details
Target Gene Details
Entrez Gene ID: | 5626 |
Gene Name: | PROP paired-like homeobox 1 |
Gene Aliases: |
CPHD2, PROP-1 |
Location: |
Chr.5:177992235-177996242 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PROP1 | NM_006261.4 | NP_006252.3 | ||
AF076215.1 | AAC77454.1 | |||
BC069076.1 | AAH69076.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv5844n100 | Chr.5:177883324 - 178184647 on Build GRCh38 | Gain | LOC100288656 GMCL1P1 RMND5B LOC100128340 NHP2 PROP1 LOC728554 N4BP3 FAM153C |
nsv509105 | Chr.5:177884347 - 178008855 on Build GRCh38 | Insertion | LOC100288656 LOC100128340 PROP1 FAM153C |
More Information
Additional Information:
For this assay, SNP(s) [rs148607624] 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 |