Assay Details
Target Gene Details
Entrez Gene ID: | 55341 |
Gene Name: | large 60S subunit nuclear export GTPase 1 |
Gene Aliases: |
- |
Location: |
Chr.3:194640788-194672477 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 12 - Intron 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LSG1 | NM_018385.2 | NP_060855.2 | ||
XM_017006796.1 | XP_016862285.1 | |||
AK002163.1 | BAA92116.1 | |||
AK225094.1 | ||||
AL136897.1 | CAB66831.1 | |||
BC015042.1 | ||||
BC040119.1 | ||||
BC068500.1 | AAH68500.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3599208 | Chr.3:194592316 - 194799085 on Build GRCh38 | Loss | LOC100507391 TMEM44 FAM43A LSG1 |
nsv508268 | Chr.3:194618407 - 194681984 on Build GRCh38 | Deletion | TMEM44 LSG1 |
nsv519476 | Chr.3:194645278 - 194972500 on Build GRCh38 | Gain | LOC100507391 FAM43A LSG1 |
More Information
Additional Information:
For this assay, SNP(s) [rs200676501] 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 Intronic Non-exonic DGV Variation |