Assay Details
Target Gene Details
Entrez Gene ID: | 114823 |
Gene Name: | leukocyte receptor cluster member 8 |
Gene Aliases: |
pp13842 |
Location: |
Chr.19:54448719-54462046 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 13 - Intron 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LENG8 | NM_052925.3 | NP_443157.1 | ||
| XM_005278248.4 | XP_005278305.1 | |||
| XM_005278249.4 | XP_005278306.1 | |||
| XM_005278250.4 | XP_005278307.1 | |||
| XM_005278252.4 | XP_005278309.1 | |||
| XM_006722996.3 | XP_006723059.1 | |||
| XM_006722997.3 | XP_006723060.1 | |||
| XM_011526413.2 | XP_011524715.1 | |||
| XM_011526414.2 | XP_011524716.1 | |||
| XM_011526415.2 | XP_011524717.1 | |||
| AL834532.1 | CAD39188.2 | |||
| BC028048.1 | AAH28048.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv3663n100 | Chr.19:54289334 - 54592227 on Build GRCh38 | Gain |
|
| nsv953617 | Chr.19:54401196 - 54463717 on Build GRCh38 | Deletion |
|
| esv2758771 | Chr.19:54163847 - 54954956 on Build GRCh38 | Gain+Loss |
|
| nsv833878 | Chr.19:54268967 - 54518890 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs75907476] 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: |
|

Genomic Map