Assay Details
Target Gene Details
Entrez Gene ID: | 54896 |
Gene Name: | PQ loop repeat containing 2 |
Gene Aliases: |
- |
Location: |
Chr.1:19312246-19332611 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PQLC2 | NM_001040125.1 | NP_001035214.1 | ||
NM_001040126.1 | NP_001035215.1 | |||
NM_001287531.1 | NP_001274460.1 | |||
NM_017765.2 | NP_060235.2 | |||
NR_109848.1 | ||||
XM_005245916.2 | XP_005245973.1 | |||
XM_006710710.2 | XP_006710773.1 | |||
XM_006710711.2 | XP_006710774.1 | |||
XM_011541634.2 | XP_011539936.1 | |||
AK000327.1 | BAA91088.1 | |||
AK125580.1 | ||||
AK130171.1 | BAC85296.1 | |||
AK130175.1 | BAC85298.1 | |||
AK172745.1 | BAD18732.1 | |||
BC015324.1 | AAH15324.1 | |||
DA202894.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs111873554] 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 non-DGV Variation |