Assay Details
Target Gene Details
Entrez Gene ID: | 8538 |
Gene Name: | BARX homeobox 2 |
Gene Aliases: |
- |
Location: |
Chr.11:129375237-129452279 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BARX2 | NM_003658.4 | NP_003649.2 | ||
XM_011543044.2 | XP_011541346.1 | |||
AF031924.1 | AAC04705.1 | |||
AJ243512.1 | CAB50736.1 | |||
BC069378.1 | AAH69378.1 | |||
BC111432.1 | ||||
BC111572.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1036787 | Chr.11:129345003 - 129455467 on Build GRCh38 | Gain | BARX2 |
nsv1046731 | Chr.11:129228206 - 129415243 on Build GRCh38 | Gain | ARHGAP32 BARX2 |
More Information
Additional Information:
For this assay, SNP(s) [rs73024965] 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 |