Assay Details
Target Gene Details
Entrez Gene ID: | 120227 |
Gene Name: | cytochrome P450 family 2 subfamily R member 1 |
Gene Aliases: |
- |
Location: |
Chr.11:14877436-14898913 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CYP2R1 | XM_011519898.2 | 1 | 4348 | XP_011518200.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3625429 | Chr.11:14852130 - 14898409 on Build GRCh38 | Gain |
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esv3891931 | Chr.11:14839971 - 14950061 on Build GRCh38 | Loss |
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nsv832071 | Chr.11:14854876 - 15027624 on Build GRCh38 | Loss |
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esv3578250 | Chr.11:14350967 - 14976647 on Build GRCh38 | Gain |
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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) [rs115156120,rs116426803] 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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