Assay Details
Target Gene Details
Entrez Gene ID: | 1947 |
Gene Name: | ephrin B1 |
Gene Aliases: |
CFND, CFNS, EFB1, EFL3, EPLG2, Elk-L, LERK2 |
Location: |
Chr.X:68828997-68842164 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EFNB1 | NM_004429.4 | NP_004420.1 | ||
| AK311197.1 | ||||
| BC016649.1 | AAH16649.1 | |||
| BC052979.1 | AAH52979.1 | |||
| BU172498.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv516469 | Chr.X:68640253 - 68949573 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs200409757] 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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Genomic Map