Genomic Map
Back To TopAssay 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 Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FCRLA | NM_001184866.1 | NP_001171795.1 | ||
| NM_001184867.1 | NP_001171796.1 | |||
| NM_001184870.1 | NP_001171799.1 | |||
| NM_001184871.1 | NP_001171800.1 | |||
| NM_001184872.1 | NP_001171801.1 | |||
| NM_001184873.1 | NP_001171802.1 | |||
| NM_032738.3 | NP_116127.3 | |||
| XM_006711581.3 | XP_006711644.1 | |||
| XM_011510064.1 | XP_011508366.1 | |||
| XM_011510065.1 | XP_011508367.1 | |||
| XM_011510066.1 | XP_011508368.1 | |||
| AF329489.1 | AAL23899.1 | |||
| AF329491.1 | AAL23901.1 | |||
| AF329493.1 | AAL23903.1 | |||
| AF329494.1 | AAL23904.1 | |||
| AF329495.1 | AAL23905.1 | |||
| AF390036.1 | AAL27307.1 | |||
| AF426461.1 | AAL58111.1 | |||
| AF531423.1 | AAM97591.1 | |||
| AY091642.2 | AAM13980.2 | |||
| AY358348.1 | AAQ88714.1 | |||
| BC006521.2 | ||||
| BM471887.1 |
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 |
 FCRLB
DUSP12
HSPA6
RPL31P11
FCGR2A
ATF6
FCGR2C
FCRLA
HSPA7
FCGR3A
LOC100422526
FCGR2B
FCGR3B
|
| nsv548075 | Chr.1:161677017 - 161915562 on Build GRCh38 | Gain |
FCRLA
FCRLB
DUSP12
RPL31P11
ATF6
LOC100422526
FCGR2B
|
| esv2758972 | Chr.1:161374465 - 161711762 on Build GRCh38 | Gain+Loss |
FCRLA
HSPA6
HSPA7
RPL31P11
FCGR2A
FCGR3A
FCGR2C
FCGR2B
FCGR3B
|
| esv33393 | Chr.1:161508891 - 162110537 on Build GRCh38 | Gain+Loss |
FCRLB
DUSP12
NOS1AP
HSPA6
RPL31P11
FCGR2A
ATF6
FCGR2C
FCRLA
OLFML2B
HSPA7
FCGR3A
LOC100422526
FCGR2B
FCGR3B
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs113214681] 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
|
Panther Classification:
Gene Ontology Categories:
Back To Top