Assay Details
Target Gene Details
Entrez Gene ID: | 6671 |
Gene Name: | Sp4 transcription factor |
Gene Aliases: |
HF1B, SPR-1 |
Location: |
Chr.7:21428071-21514761 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SP4 | NM_001326542.1 | NP_001313471.1 | ||
NM_001326543.1 | NP_001313472.1 | |||
NM_003112.4 | NP_003103.2 | |||
XM_005249828.2 | XP_005249885.1 | |||
XM_005249829.3 | XP_005249886.1 | |||
XM_011515486.2 | XP_011513788.1 | |||
XM_011515487.2 | XP_011513789.1 | |||
XM_017012557.1 | XP_016868046.1 | |||
AK289728.1 | ||||
BC109300.1 | AAI09301.1 | |||
BC109301.1 | AAI09302.1 | |||
X68561.1 | CAA48563.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv830921 | Chr.7:21449482 - 21648398 on Build GRCh38 | Gain | DNAH11 SP4 MIR1183 |
esv3571692 | Chr.7:21454745 - 21468111 on Build GRCh38 | Loss | SP4 |
More Information
Additional Information:
For this assay, SNP(s) [rs114244665] 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 |