Assay Details
Target Gene Details
Entrez Gene ID: | 656 |
Gene Name: | bone morphogenetic protein 8b |
Gene Aliases: |
BMP8, OP2 |
Location: |
Chr.1:39757182-39788861 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BMP8B | NM_001720.3 | 1 | 121 | NP_001711.2 |
| AY303955.1 | 1 | 121 | AAP74560.1 | |
| BC108678.1 | 1 | 109 | AAI08679.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2758933 | Chr.1:39759471 - 40194760 on Build GRCh38 | Loss |
|
| dgv152n100 | Chr.1:39693156 - 39800418 on Build GRCh38 | Gain |
|
| dgv153n100 | Chr.1:39715819 - 39848248 on Build GRCh38 | Gain |
|
| nsv1075454 | Chr.1:39788227 - 39789528 on Build GRCh38 | Deletion |
|
| nsv546063 | Chr.1:39719061 - 39841226 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs117002695] 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: |
|

Genomic Map