Assay Details
Target Gene Details
Entrez Gene ID: | 169792 |
Gene Name: | GLIS family zinc finger 3 |
Gene Aliases: |
NDH, ZNF515 |
Location: |
Chr.9:3824127-4310694 on Build GRCh38 |
Assay Gene Location: | Within Exon 19 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GLIS3 | NM_001042413.1 | 11 | 5078 | NP_001035878.1 |
NM_152629.3 | 10 | 4094 | NP_689842.3 | |
XM_005251386.4 | 10 | 4637 | XP_005251443.1 | |
XM_005251387.4 | 10 | 4915 | XP_005251444.1 | |
XM_005251388.4 | 9 | 4429 | XP_005251445.1 | |
XM_011517763.2 | 11 | 4757 | XP_011516065.1 | |
XM_011517764.2 | 11 | 4587 | XP_011516066.1 | |
XM_011517766.2 | 10 | 5166 | XP_011516068.1 | |
XM_011517767.2 | 10 | 4560 | XP_011516069.1 | |
XM_017014361.1 | 10 | 4865 | XP_016869850.1 | |
AB065086.1 | 1 | 40 | BAB93523.1 | |
AB209404.1 | 8 | 2687 | BAD92641.1 | |
AK055907.1 | 1 | 1315 | ||
AK075059.1 | ||||
AK096318.1 | 8 | 2721 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1028973 | Chr.9:3789264 - 3856678 on Build GRCh38 | Loss | GLIS3 |
More Information
Additional Information:
For this assay, SNP(s) [rs80030970] 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 |