Assay Details
Target Gene Details
Entrez Gene ID: | 22801 |
Gene Name: | integrin subunit alpha 11 |
Gene Aliases: |
HsT18964 |
Location: |
Chr.15:68297433-68432312 on Build GRCh38 |
Assay Gene Location: | Within Exon 31 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ITGA11 | NM_001004439.1 | 30 | 4428 | NP_001004439.1 |
XM_005254228.3 | 28 | 4650 | XP_005254285.1 | |
XM_011521363.2 | 28 | 4380 | XP_011519665.1 | |
AF109681.1 | 30 | 4416 | AAF01258.1 | |
AF111799.1 | AAL39001.1 | |||
AK095863.1 | 13 | 1774 | ||
AL359064.1 | 8 | 1484 | CAB94392.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv33024 | Chr.15:68299521 - 68336679 on Build GRCh38 | Gain | ITGA11 |
esv2760036 | Chr.15:68245734 - 68522324 on Build GRCh38 | Loss | ITGA11 CORO2B FEM1B |
More Information
Additional Information:
For this assay, SNP(s) [rs76875722] 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 |