Assay Details
Target Gene Details
Entrez Gene ID: | 92749 |
Gene Name: | dynein regulatory complex subunit 1 |
Gene Aliases: |
C2orf39, CCDC164, CILD21 |
Location: |
Chr.2:26401912-26456713 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DRC1 | NM_145038.4 | NP_659475.2 | ||
| XM_005264637.3 | XP_005264694.1 | |||
| XM_017005271.1 | XP_016860760.1 | |||
| AK057222.1 | BAB71385.1 | |||
| AK289953.1 | ||||
| AK307094.1 | ||||
| AL833892.1 | CAD38748.1 | |||
| DB021259.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2657536 | Chr.2:26398037 - 26425785 on Build GRCh38 | Deletion |
|
| esv3590122 | Chr.2:26398041 - 26425725 on Build GRCh38 | Loss |
|
| esv33316 | Chr.2:25440017 - 26672800 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs74936036] 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