Assay Details
Target Gene Details
Entrez Gene ID: | 121340 |
Gene Name: | Sp7 transcription factor |
Gene Aliases: |
OI11, OI12, OSX, osterix |
Location: |
Chr.12:53326575-53344793 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SP7 | NM_001173467.2 | NP_001166938.1 | ||
NM_001300837.1 | NP_001287766.1 | |||
NM_152860.1 | NP_690599.1 | |||
XM_011537900.2 | XP_011536202.1 | |||
AF466179.1 | AAO33377.1 | |||
AF477981.1 | AAL84281.1 | |||
AK128520.1 | ||||
AY150673.1 | AAN85556.1 | |||
AY150674.1 | AAN85557.1 | |||
BC101549.1 | AAI01550.1 | |||
BC113613.1 | ||||
HY020346.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv517066 | Chr.12:53006394 - 53340722 on Build GRCh38 | Loss | IGFBP6 AAAS EIF4B MFSD5 SP7 SOAT2 SPRYD3 ZNF740 LOC283335 PFDN5 CSAD C12orf10 ESPL1 RARG TNS2 MIR6757 ITGB7 |
More Information
Additional Information:
For this assay, SNP(s) [rs375860385] 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 |