Assay Details
Target Gene Details
Entrez Gene ID: | 57666 |
Gene Name: | fibrosin like 1 |
Gene Aliases: |
- |
Location: |
Chr.12:132490440-132585188 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FBRSL1 | NM_001142641.1 | NP_001136113.1 | ||
XM_005266171.3 | XP_005266228.1 | |||
XM_005266173.3 | XP_005266230.1 | |||
XM_005266175.3 | XP_005266232.1 | |||
XM_005266176.3 | XP_005266233.1 | |||
XM_005266177.3 | XP_005266234.1 | |||
XM_005266181.3 | XP_005266238.1 | |||
XM_011534803.2 | XP_011533105.1 | |||
XM_011534804.2 | XP_011533106.1 | |||
XM_011534805.2 | XP_011533107.1 | |||
XM_011534806.2 | XP_011533108.1 | |||
XM_011534807.2 | XP_011533109.1 | |||
XM_011534808.2 | XP_011533110.1 | |||
XM_011534809.2 | XP_011533111.1 | |||
XM_011534810.2 | XP_011533112.1 | |||
XM_011534812.2 | XP_011533114.1 | |||
XM_011534816.2 | XP_011533118.1 | |||
AB046765.2 | BAB13371.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv509494 | Chr.12:132421136 - 132526299 on Build GRCh38 | Insertion | LOC105370092 FBRSL1 MUC8 |
nsv470334 | Chr.12:132478070 - 132553706 on Build GRCh38 | Loss | FBRSL1 LOC100996573 |
nsv952512 | Chr.12:132192256 - 132711214 on Build GRCh38 | Deletion | LOC100130238 LOC105370092 PXMP2 FBRSL1 MIR6763 POLE P2RX2 PGAM5 LOC101928416 LRCOL1 LOC100996573 MUC8 GALNT9 |
dgv3046n54 | Chr.12:132481702 - 132614597 on Build GRCh38 | Loss | FBRSL1 LOC100996573 MIR6763 LRCOL1 |
nsv826563 | Chr.12:132125383 - 132622340 on Build GRCh38 | Gain | DDX51 LOC100130238 LOC105370092 FBRSL1 MIR6763 P2RX2 LOC101928416 LRCOL1 EP400NL LOC100996573 NOC4L MUC8 GALNT9 |
More Information
Additional Information:
For this assay, SNP(s) [rs139171569] 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 |