Assay Details
Target Gene Details
Entrez Gene ID: | 84824 |
Gene Name: | Fc receptor like A |
Gene Aliases: |
FCRL, FCRL1, FCRLM1, FCRLX, FCRLb, FCRLc1, FCRLc2, FCRLd, FCRLe, FCRX, FREB |
Location: |
Chr.1:161706972-161714352 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FCRLA | NM_001184866.1 | 6 | 1952 | NP_001171795.1 |
NM_001184867.1 | 4 | 1667 | NP_001171796.1 | |
NM_001184870.1 | 4 | 1532 | NP_001171799.1 | |
NM_001184871.1 | 2 | 1229 | NP_001171800.1 | |
NM_001184872.1 | 3 | 1514 | NP_001171801.1 | |
NM_001184873.1 | 3 | 1382 | NP_001171802.1 | |
NM_032738.3 | 5 | 1934 | NP_116127.3 | |
XM_006711581.3 | 5 | 1635 | XP_006711644.1 | |
XM_011510064.1 | 6 | 1692 | XP_011508366.1 | |
XM_011510065.1 | 5 | 1440 | XP_011508367.1 | |
XM_011510066.1 | 4 | 1564 | XP_011508368.1 | |
AF329489.1 | 5 | 1657 | AAL23899.1 | |
AF329491.1 | 3 | 1277 | AAL23901.1 | |
AF426461.1 | 5 | 1702 | AAL58111.1 | |
AF531423.1 | 5 | 1934 | AAM97591.1 | |
AY091642.2 | 6 | 1659 | AAM13980.2 | |
AY358348.1 | 5 | 1649 | AAQ88714.1 | |
BC006521.2 | 5 | 1749 | ||
BX649184.1 | 3 | 2492 | CAE46202.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv428257 | Chr.1:161436525 - 161898473 on Build GRCh38 | Loss | FCGR3A FCGR2B LOC100422526 ATF6 HSPA7 RPL31P11 FCGR2C HSPA6 FCRLA FCGR3B FCRLB DUSP12 FCGR2A |
nsv548075 | Chr.1:161677017 - 161915562 on Build GRCh38 | Gain | FCGR2B LOC100422526 RPL31P11 FCRLA ATF6 FCRLB DUSP12 |
esv33393 | Chr.1:161508891 - 162110537 on Build GRCh38 | Gain+Loss | NOS1AP FCGR3A FCGR2B LOC100422526 ATF6 HSPA7 RPL31P11 OLFML2B FCGR2C HSPA6 FCRLA FCGR3B FCRLB DUSP12 FCGR2A |
More Information
Additional Information:
For this assay, SNP(s) [rs115102512] 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 Exonic DGV Variation |