accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other FCRLA CNV Assays ›
Gene Symbol
FCRLA
Assay Reference Genome
Location

Chr.1:161713941 on build GRCh38
Cytoband
1q23.3
Assay ID Hs03047270_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

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

Back To Top

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

Panther Classification:

Gene Ontology Categories:

Function(s)


Back To Top

Related Products