Assay Details
Target Gene Details
Entrez Gene ID: | 6670 |
Gene Name: | Sp3 transcription factor |
Gene Aliases: |
SPR2 |
Location: |
Chr.2:173906459-173965702 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SP3 | NM_001017371.4 | NP_001017371.3 | ||
NM_001172712.1 | NP_001166183.1 | |||
NM_003111.4 | NP_003102.1 | |||
AB209334.1 | BAD92571.1 | |||
AK304199.1 | ||||
AY070137.1 | AAL58088.1 | |||
AY441957.1 | AAR30505.1 | |||
AY441958.1 | AAR30506.1 | |||
BC042945.2 | AAH42945.2 | |||
BC126414.1 | ||||
BC143928.1 | ||||
M97191.2 | AAA36630.2 | |||
X68560.1 | CAA48562.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv953518 | Chr.2:173922873 - 173963172 on Build GRCh38 | Duplication | SP3 |
More Information
Additional Information:
For this assay, SNP(s) [rs73028254] 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 |