Assay Details
Target Gene Details
Entrez Gene ID: | 57633 |
Gene Name: | leucine rich repeat neuronal 1 |
Gene Aliases: |
FIGLER3, NLRR-1 |
Location: |
Chr.3:3799431-3849834 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LRRN1 | NM_001324188.1 | NP_001311117.1 | ||
NM_001324189.1 | NP_001311118.1 | |||
NM_020873.6 | NP_065924.3 | |||
AK291717.1 | ||||
BC034947.2 | AAH34947.1 | |||
DA736067.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1000460 | Chr.3:3399757 - 3993339 on Build GRCh38 | Gain | LOC100130207 LRRN1 |
nsv1011650 | Chr.3:3797741 - 3934721 on Build GRCh38 | Loss | LOC100130207 LRRN1 |
esv3893637 | Chr.3:3512223 - 3972206 on Build GRCh38 | Loss | LOC100130207 LRRN1 |
esv2752001 | Chr.3:3539056 - 3858107 on Build GRCh38 | Gain | LOC100130207 LRRN1 |
nsv589396 | Chr.3:3203825 - 3821595 on Build GRCh38 | Gain | LOC100130207 LRRN1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73016429] 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 |