Assay Details
Target Gene Details
Entrez Gene ID: | 22924 |
Gene Name: | microtubule associated protein RP/EB family member 3 |
Gene Aliases: |
EB3, EBF3, EBF3-S, RP3 |
Location: |
Chr.2:26970371-27027219 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MAPRE3 | NM_012326.3 | NP_036458.2 | ||
XM_006711967.3 | XP_006712030.1 | |||
XM_017003597.1 | XP_016859086.1 | |||
AB025186.1 | BAA82958.1 | |||
AK312342.1 | ||||
BC011557.1 | AAH11557.1 | |||
DC417465.1 | ||||
Y11174.1 | CAA72060.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv6744n54 | Chr.2:26973431 - 27151141 on Build GRCh38 | Loss | AGBL5 TRA-AGC8-1 MAPRE3 LOC100129724 ABHD1 PRR30 OST4 PREB TMEM214 EMILIN1 CGREF1 AGBL5-AS1 TCF23 KHK |
nsv455974 | Chr.2:26989775 - 27128411 on Build GRCh38 | Loss | AGBL5 TRA-AGC8-1 TMEM214 EMILIN1 MAPRE3 CGREF1 LOC100129724 AGBL5-AS1 KHK ABHD1 OST4 |
More Information
Additional Information:
For this assay, SNP(s) [rs182474590] 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 |