Display Info New header:
tfpt-header-footer.tfcom-eks-na-comerce-gateway-prd.commerceprod.thermofisher.net cookie.CK_ISO_CODE.value:us
cookie.CK_LANG_CODE.value:en
cookie.CK_DISPLAY_TYPE.value:
pageContext.request:org.apache.struts2.dispatcher.StrutsRequestWrapper@445d6ae1
Request attributes: pageContext.request.scheme:http(not used)
syndicationProtocol:https
syndicationExtensionPrefix:
syndicationDisplayType:/anonymous enableSimpleHeaderValue:

System Message

OKCancel
See other NR1H2 CNV Assays ›
Gene Symbol
NR1H2
Assay Reference Genome
Location

Chr.19:50378791 on build GRCh38
Cytoband
19q13.33
Assay ID Hs02219027_cn
Size
Availability Made To Order
Catalog # 4400291
Price (USD) 457.00
Your Price
Online offer (USD):424.65
424.65
Check your price ›

Genomic Map

Build 38.2 Human Chr.19: Hs02219027_cn
Created with Raphaël 2.1.2NR1H2POLD1NR1H2POLD150,356,00050,357,00050,358,00050,359,00050,360,00050,361,00050,362,00050,363,00050,364,00050,365,00050,366,00050,367,00050,368,00050,369,00050,370,00050,371,00050,372,00050,373,00050,374,00050,375,00050,376,00050,377,00050,378,00050,379,00050,380,00050,381,00050,382,00050,383,00050,384,00050,385,00050,386,00050,387,00050,388,00050,389,00050,390,00050,391,00050,392,00050,393,00050,394,00050,395,00050,396,00050,397,00050,398,00050,399,00050,400,00050,401,00050,402,00050,403,000
Back To Top

Assay Details

Target Gene Details

Entrez Gene ID:

 7376

Gene Name:

 nuclear receptor subfamily 1 group H member 2

Gene Aliases:

 LXR-b, LXRB, NER, NER-I, RIP15, UNR

Location:

 Chr.19:50376423-50383028 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 6 - Intron 6
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NR1H2 NM_001256647.1 NP_001243576.1
NM_007121.5 NP_009052.3
AB307697.1
AK091535.1
AK290855.1
AK297978.1
BC007790.1 AAH07790.1
BC033500.1 AAH33500.1
BC047750.2 AAH47750.1
BC074500.1 AAH74500.1
CR456706.1 CAG32987.1
CR749648.1 CAH18442.1
HQ692835.1
U07132.1 AAA61783.1
U14534.1 AAA58594.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1066389 Chr.19:50319151 - 50453251 on Build GRCh38 Gain POLD1 NAPSB NR1H2 KCNC3 MYBPC2 NAPSA SPIB

Back To Top

More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products

Display Info:
cookie.CK_ISO_CODE.value:us
cookie.CK_LANG_CODE.value:en
cookie.CK_DISPLAY_TYPE.value:
pageContext.request.scheme:http(not used)
syndicationProtocol:https
syndicationExtensionPrefix:
syndicationDisplayType:/anonymous