Assay Details
Target Gene Details
Entrez Gene ID: | 79370 |
Gene Name: | BCL2 like 14 |
Gene Aliases: |
BCLG |
Location: |
Chr.12:12049844-12099695 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BCL2L14 | NM_030766.1 | NP_110393.1 | ||
NM_138722.1 | NP_620048.1 | |||
NM_138723.1 | NP_620049.1 | |||
XM_006719151.3 | XP_006719214.1 | |||
XM_011520848.1 | XP_011519150.1 | |||
XM_011520849.1 | XP_011519151.1 | |||
XM_017019963.1 | XP_016875452.1 | |||
AF281254.1 | AAG59793.1 | |||
AF281255.1 | AAG59794.1 | |||
AK223415.1 | BAD97135.1 | |||
AK292995.1 | ||||
BC025778.1 | AAH25778.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1046355 | Chr.12:11501836 - 12890185 on Build GRCh38 | Loss | LOC105369662 DUSP16 BCL2L14 APOLD1 CREBL2 MIR1244-4 LOC100506248 ETV6 MIR613 LRP6 LINC01252 DDX47 GPR19 BORCS5 CDKN1B LOH12CR2 MANSC1 RPL13AP20 |
More Information
Additional Information:
For this assay, SNP(s) [rs75691667] 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 |