Assay Details
Target Gene Details
Entrez Gene ID: | 653499 |
Gene Name: | galectin 7B |
Gene Aliases: |
GAL7, Gal-7, HKL-14, LGALS7, PI7 |
Location: |
Chr.19:38789210-38791754 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LGALS7B | NM_001042507.3 | NP_001035972.1 | ||
| AW015224.1 | ||||
| BC042911.2 | AAH42911.2 | |||
| BC061588.1 | AAH61588.1 | |||
| BC073743.1 | AAH73743.1 | |||
| L07769.1 | AAA67899.1 | |||
| U06643.1 | AAA86820.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1063592 | Chr.19:38767337 - 38796625 on Build GRCh38 | Gain |
|
| nsv963045 | Chr.19:38789906 - 38792508 on Build GRCh38 | Duplication |
|
| nsv9720 | Chr.19:38786691 - 38792736 on Build GRCh38 | Gain |
|
| dgv3527n100 | Chr.19:38758419 - 38812203 on Build GRCh38 | Gain |
|
| nsv1058132 | Chr.19:38788882 - 38812203 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76477826] 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