Assay Details
Target Gene Details
Entrez Gene ID: | 6662 |
Gene Name: | SRY-box 9 |
Gene Aliases: |
CMD1, CMPD1, SRA1, SRXX2, SRXY10 |
Location: |
Chr.17:72121020-72126420 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SOX9 | NM_000346.3 | 3 | 2866 | NP_000337.1 |
Z46629.1 | 3 | 2853 | CAA86598.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833530 | Chr.17:72033949 - 72232973 on Build GRCh38 | Gain+Loss | LINC01152 LOC102723517 LOC101928205 SOX9-AS1 SOX9 |
esv3573809 | Chr.17:71977779 - 72157070 on Build GRCh38 | Gain | LINC01152 LOC102723517 LOC102723505 LOC101928205 SOX9-AS1 SOX9 |
More Information
Additional Information:
For this assay, SNP(s) [rs74999341] 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 |