Assay Details
Target Gene Details
Entrez Gene ID: | 388611 |
Gene Name: | CD164 molecule like 2 |
Gene Aliases: |
EAPG6122, UNQ6122 |
Location: |
Chr.1:27379100-27383333 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CD164L2 | NM_207397.3 | NP_997280.2 | ||
XM_005245868.3 | XP_005245925.2 | |||
XM_011541441.1 | XP_011539743.1 | |||
AY358761.1 | AAQ89121.1 | |||
BC137466.1 | ||||
DB114521.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv526051 | Chr.1:27284255 - 27445496 on Build GRCh38 | Gain | ACTG1P20 GPR3 FCN3 WASF2 TMEM222 MAP3K6 CD164L2 WDTC1 SYTL1 |
nsv516766 | Chr.1:27335744 - 27405147 on Build GRCh38 | Loss | GPR3 FCN3 WASF2 TMEM222 MAP3K6 CD164L2 SYTL1 |
More Information
Additional Information:
For this assay, SNP(s) [rs76651420] 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 Non-exonic DGV Variation |