Assay Details
Target Gene Details
Entrez Gene ID: | 149499 |
Gene Name: | leucine rich repeat containing 71 |
Gene Aliases: |
C1orf92 |
Location: |
Chr.1:156920608-156941208 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LRRC71 | NM_144702.2 | NP_653303.2 | ||
XM_005244926.3 | XP_005244983.1 | |||
XM_005244927.3 | XP_005244984.1 | |||
XM_005244928.2 | XP_005244985.1 | |||
XM_006711185.3 | XP_006711248.1 | |||
XM_006711186.3 | XP_006711249.1 | |||
XM_006711187.3 | XP_006711250.1 | |||
XM_011509239.2 | XP_011507541.1 | |||
XM_011509240.2 | XP_011507542.1 | |||
XM_017000459.1 | XP_016855948.1 | |||
XM_017000460.1 | XP_016855949.1 | |||
XM_017000461.1 | XP_016855950.1 | |||
XM_017000462.1 | XP_016855951.1 | |||
AK057446.1 | BAB71490.1 | |||
AK292342.1 | ||||
BC033790.1 | AAH33790.1 | |||
BU689904.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3890682 | Chr.1:156899922 - 156951428 on Build GRCh38 | Loss |
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nsv831659 | Chr.1:156771159 - 156980204 on Build GRCh38 | Loss |
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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) [rs117542119] 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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Panther Classification:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)