Genomic Map
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Target Gene Details
Entrez Gene ID: | 101929152 |
Gene Name: | P3H2 antisense RNA 1 |
Gene Aliases: |
LEPREL1-AS1 |
Location: |
Chr.3:190120964-190144846 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| P3H2-AS1 | NR_126419.1 | |||
| BM017065.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1014822 | Chr.3:190065059 - 190464556 on Build GRCh38 | Gain |
 CLDN16
TMEM207
P3H2
P3H2-AS1
CLDN1
|
| nsv525254 | Chr.3:190137954 - 190141334 on Build GRCh38 | Loss |
P3H2-AS1
|
| esv3893843 | Chr.3:190075998 - 191094501 on Build GRCh38 | Gain |
SNAR-I
IL1RAP
CLDN16
TMEM207
P3H2
P3H2-AS1
CLDN1
GMNC
|
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Additional Information:
For this assay, SNP(s) [rs143232407] 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
|
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