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 | TRIT1 CAP1 MFSD2A OXCT2 MYCL LOC101929536 RLF PPIE BMP8B PPT1 |
dgv152n100 | Chr.1:39693156 - 39800418 on Build GRCh38 | Gain | OXCT2 LOC101929536 PPIE BMP8B |
dgv153n100 | Chr.1:39715819 - 39848248 on Build GRCh38 | Gain | TRIT1 OXCT2 LOC101929536 PPIE BMP8B |
nsv1075454 | Chr.1:39788227 - 39789528 on Build GRCh38 | Deletion | LOC101929536 BMP8B |
nsv546063 | Chr.1:39719061 - 39841226 on Build GRCh38 | Gain | TRIT1 OXCT2 LOC101929536 PPIE BMP8B |
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: |
Intragenic Exonic DGV Variation |