Assay Details
Target Gene Details
Entrez Gene ID: | 4920 |
Gene Name: | receptor tyrosine kinase like orphan receptor 2 |
Gene Aliases: |
BDB, BDB1, NTRKR2 |
Location: |
Chr.9:91722596-91950206 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ROR2 | NM_004560.3 | 9 | 3164 | NP_004551.2 |
XM_005252008.4 | 9 | 3129 | XP_005252065.1 | |
XM_005252009.3 | 3 | 1870 | XP_005252066.1 | |
XM_006717121.3 | 9 | 3786 | XP_006717184.1 | |
XM_017014762.1 | 9 | 4861 | XP_016870251.1 | |
XM_017014763.1 | 9 | 3040 | XP_016870252.1 | |
AB209154.1 | 11 | 3433 | BAD92391.1 | |
BC130522.1 | 9 | 3052 | ||
M97639.1 | 9 | 3164 | AAA60276.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1045332 | Chr.9:91590379 - 91893734 on Build GRCh38 | Loss | ROR2 MIR3910-2 MIR3910-1 |
esv3576683 | Chr.9:91651711 - 91758339 on Build GRCh38 | Gain | ROR2 |
More Information
Additional Information:
For this assay, SNP(s) [rs140581955] 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 DGV Variation |