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See other LRRC27 CNV Assays ›
Gene Symbol
LRRC27
Assay Reference Genome
Location

Chr.10:132339708 on build GRCh38
Cytoband
10q26.3
Assay ID Hs05227281_cn
Size
Availability Made To Order
Catalog # 4400291
Price 475.00
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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 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LRRC27 NM_001143757.1 NP_001137229.1
NM_001143758.1 NP_001137230.1
NM_001143759.1 NP_001137231.1
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_017016691.1 XP_016872180.1
XM_017016692.1 XP_016872181.1
XM_017016693.1 XP_016872182.1
XM_017016694.1 XP_016872183.1
AB051461.1
AK093250.1 BAC04108.1
AK097418.1
AK098652.1 BAC05366.1
AK295953.1
AK301422.1
BC050097.1 AAH50097.1
DA658738.1
DC352688.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1054569 Chr.10:132009350 - 132351508 on Build GRCh38 Gain JAKMIP3 STK32C LRRC27 DPYSL4
esv3624988 Chr.10:132338306 - 132366249 on Build GRCh38 Gain LRRC27
nsv1051555 Chr.10:132295188 - 132415461 on Build GRCh38 Gain PWWP2B STK32C LRRC27
esv3624986 Chr.10:132322882 - 132551350 on Build GRCh38 Gain PWWP2B STK32C C10orf91 LOC107984282 LRRC27 INPP5A LOC105378568
esv2761642 Chr.10:132048518 - 132365985 on Build GRCh38 Gain JAKMIP3 STK32C LRRC27 DPYSL4
nsv1054934 Chr.10:130334322 - 133158679 on Build GRCh38 Gain JAKMIP3 MIR378C LINC01164 ADGRA1 LINC01168 LINC01167 BNIP3 C10orf91 LOC107984282 ADGRA1-AS1 DPYSL4 INPP5A PWWP2B NKX6-2 CFAP46 LINC01166 TCERG1L STK32C LRRC27 LOC105378568 TCERG1L-AS1 PPP2R2D
nsv1052405 Chr.10:132336481 - 132390781 on Build GRCh38 Gain LRRC27

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

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