Product Details
- Assay Reference Genome
Location
Chr.X:22047177 on build GRCh38
- Cytoband
- Xp22.11
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs112836831] 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.
Target Gene Details
- Entrez Gene ID
- 5251
- Gene Symbol
- PHEX
- Gene Name
- phosphate regulating endopeptidase homolog, X-linked
- Gene Aliases
- HPDR, HPDR1, HYP, HYP1, LXHR, PEX, XLH
- Location
- Chr.X:22032327-22251310 on build GRCh38
- Assay Gene Location
- Overlaps Exon 3 - Intron 3
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