Assay Details
Target Gene Details
Entrez Gene ID: | 29119 |
Gene Name: | catenin alpha 3 |
Gene Aliases: |
ARVD13, VR22 |
Location: |
Chr.10:65912518-67696217 on Build GRCh38 |
Assay Gene Location: | Within Intron 15 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CTNNA3 | NM_001127384.2 | NP_001120856.1 | ||
NM_013266.3 | NP_037398.2 | |||
XM_017016151.1 | XP_016871640.1 | |||
XM_017016152.1 | XP_016871641.1 | |||
XM_017016153.1 | XP_016871642.1 | |||
XM_017016154.1 | XP_016871643.1 | |||
XM_017016155.1 | XP_016871644.1 | |||
XM_017016156.1 | XP_016871645.1 | |||
AF091606.1 | AAF21801.1 | |||
AK289756.1 | ||||
AK313882.1 | ||||
BC065819.1 | AAH65819.1 |
Target Gene Details
Entrez Gene ID: | 101928961 |
Gene Name: | uncharacterized LOC101928961 |
Gene Aliases: |
- |
Location: |
Chr.10:66894110-67012153 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC101928961 | NR_111911.1 | 7 | 3459 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3891850 | Chr.10:66648103 - 66920775 on Build GRCh38 | Loss | CTNNA3 LOC101928961 |
nsv1038079 | Chr.10:66630592 - 66920330 on Build GRCh38 | Loss | CTNNA3 LOC101928961 |
nsv1050214 | Chr.10:66771920 - 66946821 on Build GRCh38 | Loss | CTNNA3 LOC101928961 LRRTM3 |
More Information
Additional Information:
For this assay, SNP(s) [rs111948569] 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 Intronic Non-exonic DGV Variation |