Assay Details
Target Gene Details
Entrez Gene ID: | 22919 |
Gene Name: | microtubule associated protein RP/EB family member 1 |
Gene Aliases: |
EB1 |
Location: |
Chr.20:32819780-32850405 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MAPRE1 | NM_012325.2 | NP_036457.1 | ||
XM_011528696.2 | XP_011526998.1 | |||
AK297273.1 | ||||
AK312590.1 | ||||
BC106068.1 | AAI06069.1 | |||
BC109281.3 | AAI09282.1 | |||
BC128442.1 | ||||
BJ992159.1 | ||||
U24166.1 | AAC09471.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1056411 | Chr.20:32469234 - 33355029 on Build GRCh38 | Loss | LOC101929698 BPIFB2 BPIFB4 COMMD7 BPIFB1 BPIFA2 C20orf203 BPIFB6 EFCAB8 MAPRE1 SUN5 BPIFA3 BPIFA4P DNMT3B NOL4L BPIFA1 BPIFB3 LOC105372714 LOC149950 |
nsv833957 | Chr.20:32755316 - 32907992 on Build GRCh38 | Gain+Loss | DNMT3B EFCAB8 MAPRE1 |
More Information
Additional Information:
For this assay, SNP(s) [rs79575953] 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 |