Assay Details
Target Gene Details
Entrez Gene ID: | 142685 |
Gene Name: | ankyrin repeat and SOCS box containing 15 |
Gene Aliases: |
- |
Location: |
Chr.7:123567003-123637900 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ASB15 | NM_001290258.1 | NP_001277187.1 | ||
NM_080928.4 | NP_563616.3 | |||
XM_005250146.4 | XP_005250203.1 | |||
XM_011515816.2 | XP_011514118.1 | |||
XM_011515817.2 | XP_011514119.1 | |||
XM_011515818.2 | XP_011514120.1 | |||
XM_011515819.2 | XP_011514121.1 | |||
XM_011515820.2 | XP_011514122.1 | |||
XM_011515821.2 | XP_011514123.1 | |||
XM_017011756.1 | XP_016867245.1 | |||
XM_017011757.1 | XP_016867246.1 | |||
AF428257.1 | AAP97297.1 | |||
AK125360.1 | BAC86146.1 | |||
BC100874.2 | AAI00875.1 | |||
BC100875.2 | AAI00876.1 | |||
BC100876.1 | ||||
BC100877.2 | AAI00878.1 |
Target Gene Details
Entrez Gene ID: | 102724555 |
Gene Name: | uncharacterized LOC102724555 |
Gene Aliases: |
- |
Location: |
Chr.7:123614161-123624957 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC102724555 | NR_111922.1 | |||
DB024487.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831116 | Chr.7:123447558 - 123619922 on Build GRCh38 | Gain+Loss | LOC102724555 IQUB NDUFA5 ASB15 |
esv3891198 | Chr.7:121885430 - 123886905 on Build GRCh38 | Gain | LMOD2 WASL LOC102724555 FEZF1 SLC13A1 RNF148 PTPRZ1 IQUB HYAL4 FEZF1-AS1 NDUFA5 CADPS2 RNF133 AASS ASB15 HYALP1 TAS2R16 |
More Information
Additional Information:
For this assay, SNP(s) [rs146637776] 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 Intronic Non-exonic DGV Variation |