Assay Details
Target Gene Details
Entrez Gene ID: | 100289388 |
Gene Name: | KCTD21 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.11:78139793-78173977 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
KCTD21-AS1 | NR_102280.1 | |||
NR_102281.1 | ||||
DA156609.1 | ||||
DA737651.1 | ||||
DA814941.1 | ||||
DB082989.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv520740 | Chr.11:77842592 - 78286890 on Build GRCh38 | Gain | KCTD14 KCTD21-AS1 RSF1 NDUFC2-KCTD14 ALG8 GAB2 NDUFC2 USP35 AAMDC KCTD21 INTS4 THRSP |
nsv516503 | Chr.11:78145131 - 78209884 on Build GRCh38 | Loss | KCTD21-AS1 USP35 KCTD21 |
nsv1047928 | Chr.11:78114229 - 78166323 on Build GRCh38 | Gain | KCTD21-AS1 ALG8 |
More Information
Additional Information:
For this assay, SNP(s) [rs111306477,rs115210618] 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 |