Assay Details
Target Gene Details
Entrez Gene ID: | 84465 |
Gene Name: | multiple EGF like domains 11 |
Gene Aliases: |
- |
Location: |
Chr.15:65895296-66253737 on Build GRCh38 |
Assay Gene Location: | Within Exon 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MEGF11 | NM_032445.2 | 23 | 5225 | NP_115821.2 |
XM_017022670.1 | 24 | 5806 | XP_016878159.1 | |
XM_017022671.1 | 24 | 6566 | XP_016878160.1 | |
XM_017022672.1 | 22 | 5654 | XP_016878161.1 | |
XM_017022674.1 | 20 | 5909 | XP_016878163.1 | |
XM_017022675.1 | 20 | 5947 | XP_016878164.1 | |
AB058677.1 | 21 | 5018 | ||
AK090663.1 | 1 | 1359 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833044 | Chr.15:65766302 - 65969046 on Build GRCh38 | Loss | MEGF11 LOC646358 DENND4A RAB11A |
nsv471684 | Chr.15:65890789 - 66030069 on Build GRCh38 | Gain | MEGF11 RAB11A |
esv2760035 | Chr.15:65888447 - 66058047 on Build GRCh38 | Loss | MEGF11 MIR4311 RAB11A |
More Information
Additional Information:
For this assay, SNP(s) [rs72742822] 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 Exonic DGV Variation |