Assay Details
Target Gene Details
Entrez Gene ID: | 347744 |
Gene Name: | chromosome 6 open reading frame 52 |
Gene Aliases: |
- |
Location: |
Chr.6:10671418-10694797 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C6orf52 | NM_001145020.1 | NP_001138492.1 | ||
NR_026736.1 | ||||
NR_026737.1 | ||||
XM_006715088.3 | XP_006715151.1 | |||
XM_011514572.2 | XP_011512874.1 | |||
XM_011514574.2 | XP_011512876.1 | |||
XM_011514575.2 | XP_011512877.1 | |||
AI376550.1 | ||||
AI621292.1 | ||||
AI809192.1 | ||||
AW183566.1 | ||||
AW293245.1 | ||||
BC016820.1 | AAH16820.1 | |||
BX280692.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv966670 | Chr.6:10447438 - 10871656 on Build GRCh38 | Duplication | C6orf52 TMEM14C MAK PAK1IP1 TMEM14B LOC101928106 GCNT2 MIR5689HG |
nsv462631 | Chr.6:10449025 - 10839526 on Build GRCh38 | Gain | C6orf52 TMEM14C MAK PAK1IP1 TMEM14B LOC101928106 GCNT2 MIR5689HG |
nsv470800 | Chr.6:10538711 - 10863092 on Build GRCh38 | Gain | C6orf52 TMEM14C MAK PAK1IP1 TMEM14B GCNT2 |
nsv520853 | Chr.6:10671531 - 10724327 on Build GRCh38 | Loss | C6orf52 TMEM14C PAK1IP1 |
More Information
Additional Information:
For this assay, SNP(s) [rs76589134] 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 |