Assay Details
Target Gene Details
Entrez Gene ID: | 598 |
Gene Name: | BCL2 like 1 |
Gene Aliases: |
BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52 |
Location: |
Chr.20:31664452-31723999 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BCL2L1 | NM_001191.3 | NP_001182.1 | ||
NM_001317919.1 | NP_001304848.1 | |||
NM_001317920.1 | NP_001304849.1 | |||
NM_001317921.1 | NP_001304850.1 | |||
NM_001322239.1 | NP_001309168.1 | |||
NM_001322240.1 | NP_001309169.1 | |||
NM_001322242.1 | NP_001309171.1 | |||
NM_138578.2 | NP_612815.1 | |||
NR_134257.1 | ||||
XM_011528964.2 | XP_011527266.1 | |||
XM_017027993.1 | XP_016883482.1 | |||
AK290968.1 | ||||
BC019307.1 | AAH19307.1 | |||
BM554265.1 | ||||
BT007208.1 | AAP35872.1 | |||
BX359456.2 | ||||
BX647525.1 | ||||
CD359906.1 | ||||
CR936637.1 | CAI56777.1 | |||
DR156871.1 | ||||
KU177938.1 | ||||
KU177939.1 | ||||
KU177940.1 | ||||
Z23115.1 | CAA80661.1 | |||
Z23116.1 | CAA80662.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv4300n100 | Chr.20:31247234 - 32033468 on Build GRCh38 | Gain | ID1 DEFB119 DEFB122 LINC00028 TTLL9 DEFB123 DEFB121 MIR3193 FOXS1 HM13-AS1 HM13 BCL2L1 REM1 ABALON COX4I2 DEFB124 DEFB118 CCM2L LOC107985416 PDRG1 DEFB116 MYLK2 DEFB117 DEFB115 TPX2 DUSP15 XKR7 |
nsv458961 | Chr.20:31305698 - 31688103 on Build GRCh38 | Gain | DEFB124 DEFB118 ID1 DEFB119 DEFB122 LINC00028 DEFB123 DEFB121 LOC107985416 MIR3193 DEFB116 DEFB117 HM13-AS1 HM13 BCL2L1 REM1 COX4I2 |
More Information
Additional Information:
For this assay, SNP(s) [rs77028352] 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 |