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 LRRC27 CNV Assays ›
Gene Symbol
LRRC27
Assay Reference Genome
Location

Chr.10:132354187 on build GRCh38
Cytoband
10q26.3
Assay ID Hs05153484_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 80313

Gene Name:

 leucine rich repeat containing 27

Gene Aliases:

 -

Location:

 Chr.10:132330063-132381506 on Build GRCh38

Assay Gene Location:

 Within Intron 12
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LRRC27 NM_001143757.1 NP_001137229.1
NM_001309474.1 NP_001296403.1
NM_030626.2 NP_085129.1
XM_006717983.2 XP_006718046.1
XM_006717984.2 XP_006718047.1
XM_011540208.1 XP_011538510.1
XM_011540209.1 XP_011538511.1
XM_011540210.2 XP_011538512.1
XM_017016690.1 XP_016872179.1
XM_017016694.1 XP_016872183.1
AB051461.1
AK091472.1
AK093250.1 BAC04108.1
AK097418.1
AK301422.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3624988 Chr.10:132338306 - 132366249 on Build GRCh38 Gain LRRC27
nsv1051555 Chr.10:132295188 - 132415461 on Build GRCh38 Gain PWWP2B LRRC27 STK32C
esv3624986 Chr.10:132322882 - 132551350 on Build GRCh38 Gain PWWP2B LOC107984282 LOC105378568 LRRC27 STK32C C10orf91 INPP5A
esv2761642 Chr.10:132048518 - 132365985 on Build GRCh38 Gain LRRC27 JAKMIP3 DPYSL4 STK32C
nsv1054934 Chr.10:130334322 - 133158679 on Build GRCh38 Gain PWWP2B CFAP46 JAKMIP3 DPYSL4 ADGRA1-AS1 STK32C LINC01167 NKX6-2 TCERG1L-AS1 MIR378C C10orf91 INPP5A ADGRA1 LINC01168 BNIP3 LOC107984282 LOC105378568 LRRC27 LINC01164 TCERG1L PPP2R2D LINC01166
nsv1052405 Chr.10:132336481 - 132390781 on Build GRCh38 Gain LRRC27
nsv7627 Chr.10:132350184 - 132375206 on Build GRCh38 Insertion LRRC27
dgv121n27 Chr.10:132345217 - 132477022 on Build GRCh38 Loss PWWP2B LOC105378568 LRRC27 C10orf91
esv3577872 Chr.10:132342397 - 132412909 on Build GRCh38 Gain PWWP2B LRRC27

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs138185074] 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

Back To Top

Related Products