Assay Details
Target Gene Details
Entrez Gene ID: | 51592 |
Gene Name: | tripartite motif containing 33 |
Gene Aliases: |
ECTO, PTC7, RFG7, TF1G, TIF1G, TIF1GAMMA, TIFGAMMA |
Location: |
Chr.1:114392777-114511160 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TRIM33 | NM_015906.3 | 20 | 5010 | NP_056990.3 |
NM_033020.2 | 19 | 4959 | NP_148980.2 | |
XM_005270936.3 | 21 | 5003 | XP_005270993.1 | |
XM_005270937.3 | 20 | 4952 | XP_005270994.1 | |
XM_011541568.2 | 21 | 5000 | XP_011539870.1 | |
XM_017001452.1 | 18 | 4285 | XP_016856941.1 | |
XM_017001453.1 | 17 | 4234 | XP_016856942.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv28734 | Chr.1:114376708 - 115005298 on Build GRCh38 | Loss | CSDE1 AMPD1 BCAS2 DENND2C NRAS TRIM33 SYCP1 SIKE1 |
More Information
Additional Information:
For this assay, SNP(s) [rs73003377] 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 |