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See other NRG3 CNV Assays ›
Gene Symbol
NRG3
Assay Reference Genome
Location

Chr.10:82229156 on build GRCh38
Cytoband
10q23.1
Assay ID Hs05213165_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 10718

Gene Name:

 neuregulin 3

Gene Aliases:

 HRG3, pro-NRG3

Location:

 Chr.10:81875298-82989979 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NRG3 NM_001010848.3 NP_001010848.2
NM_001165972.1 NP_001159444.1
NM_001165973.1 NP_001159445.1
XM_005269444.4 XP_005269501.1
XM_011539172.2 XP_011537474.1
XM_011539173.2 XP_011537475.1
XM_011539175.2 XP_011537477.1
XM_017015573.1 XP_016871062.1
XM_017015574.1 XP_016871063.1
XM_017015575.1 XP_016871064.1
XM_017015576.1 XP_016871065.1
XM_017015577.1 XP_016871066.1
XM_017015578.1 XP_016871067.1
XM_017015579.1 XP_016871068.1
XM_017015580.1 XP_016871069.1
XM_017015581.1 XP_016871070.1
XM_017015582.1 XP_016871071.1
XM_017015583.1 XP_016871072.1
XM_017015584.1 XP_016871073.1
AK122886.1
AK296563.1
BC136811.1
DQ001411.1 AAY17216.1
DQ338459.1 ABC69293.1
DQ857894.1
HM068873.1
HM068874.1
HM068875.1
HM068876.1
HM068877.1
HM068878.1
HM068879.1
HM068880.1
HM068881.1
HM068882.1
HM068883.1
HM068884.1

Target Gene Details

Entrez Gene ID:

 101929590

Gene Name:

 NRG3 antisense RNA 1

Gene Aliases:

 C10orf100, Em:AC010157.1

Location:

 Chr.10:82229014-82232920 on Build GRCh38

Assay Gene Location:
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NRG3-AS1 CF272718.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv551704 Chr.10:82136504 - 82268652 on Build GRCh38 Loss NRG3-AS1 NRG3
esv3891873 Chr.10:81025608 - 82340753 on Build GRCh38 Gain NRG3-AS1 NRG3
esv3891875 Chr.10:82171786 - 82294496 on Build GRCh38 Loss NRG3-AS1 NRG3

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More Information


Additional Information:

For this assay, SNP(s) [rs74615677] 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:

Molecular Function -

growth factor

Gene Ontology Categories:

Function(s) Process(es)


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