Assay Details
Target Gene Details
Entrez Gene ID: | 677 |
Gene Name: | ZFP36 ring finger protein like 1 |
Gene Aliases: |
BRF1, Berg36, ERF-1, ERF1, RNF162B, TIS11B, cMG1 |
Location: |
Chr.14:68787655-68796243 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZFP36L1 | NM_001244698.1 | 1 | 307 | NP_001231627.1 |
NM_001244701.1 | NP_001231630.1 | |||
NM_004926.3 | 1 | 307 | NP_004917.2 | |
AI809725.1 | 1 | 331 | ||
AK024202.1 | 1 | 1129 | ||
DA633985.1 | ||||
DA876968.1 | 1 | 252 | ||
FY210721.1 | ||||
X79066.1 | CAA55670.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1070226 | Chr.14:68788582 - 68795483 on Build GRCh38 | Deletion | ZFP36L1 |
nsv952859 | Chr.14:68788584 - 68795783 on Build GRCh38 | Deletion | ZFP36L1 |
dgv1097n106 | Chr.14:68790783 - 68795883 on Build GRCh38 | Deletion | ZFP36L1 |
More Information
Additional Information:
For this assay, SNP(s) [rs72731554] 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 |