Assay Details
Target Gene Details
Entrez Gene ID: | 64843 |
Gene Name: | ISL LIM homeobox 2 |
Gene Aliases: |
- |
Location: |
Chr.15:76336724-76342476 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ISL2 | NM_145805.2 | NP_665804.1 | ||
XM_017022505.1 | XP_016877994.1 | |||
AB593133.1 | 3 | 860 | ||
AK001022.1 | ||||
BC011967.1 | AAH11967.1 | |||
BC012136.1 | AAH12136.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2749895 | Chr.15:75415580 - 76472296 on Build GRCh38 | Deletion |
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nsv827391 | Chr.15:76334230 - 76343986 on Build GRCh38 | Gain |
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esv2749898 | Chr.15:75764003 - 77933523 on Build GRCh38 | Deletion |
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nsv1619 | Chr.15:76312275 - 76346029 on Build GRCh38 | Insertion |
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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) [rs79170365] 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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Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)