Assay Details
Target Gene Details
Entrez Gene ID: | 401 |
Gene Name: | paired like homeobox 2a |
Gene Aliases: |
ARIX, CFEOM2, FEOM2, NCAM2, PMX2A |
Location: |
Chr.11:72239077-72244176 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PHOX2A | NM_005169.3 | NP_005160.2 | ||
AK290645.1 | ||||
BC041564.1 | AAH41564.1 | |||
BQ890461.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv951038 | Chr.11:72226157 - 72253456 on Build GRCh38 | Deletion |
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esv26290 | Chr.11:72241223 - 72242546 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs117476547] 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: |
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Panther Classification:
Gene Ontology Categories:
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