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See other NCOA7 CNV Assays ›
Gene Symbol
NCOA7
Assay Reference Genome
Location

Chr.6:125802204 on build GRCh38
Cytoband
6q22.32
Assay ID Hs06745628_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 135112

Gene Name:

 nuclear receptor coactivator 7

Gene Aliases:

 ERAP140, ESNA1, NCOA7-AS, Nbla00052, Nbla10993, TLDC4, dJ187J11.3

Location:

 Chr.6:125780948-125932030 on Build GRCh38

Assay Gene Location:

 Within Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NCOA7 NM_001122842.2 NP_001116314.1
NM_001199619.1 NP_001186548.1
NM_001199620.1 NP_001186549.1
NM_001199621.1 NP_001186550.1
NM_181782.4 NP_861447.3
XM_005266822.4 XP_005266879.1
XM_006715340.3 XP_006715403.1
XM_011535455.2 XP_011533757.1
XM_017010270.1 XP_016865759.1
XM_017010271.1 XP_016865760.1
XM_017010272.1 XP_016865761.1
XM_017010273.1 XP_016865762.1
XM_017010274.1 XP_016865763.1
AB074156.1 BAE45731.1
AB074157.1 BAE45732.1
AF493978.1 AAM27392.1
AK127512.1
AK294558.1
AK307395.1
AL832621.2 CAD90002.2
AL832628.2 CAD89948.1
BC036461.1 AAH36461.1
BC137094.1
BC137095.1
BX537385.1 CAD97627.1
DA770225.1

Target Gene Details

Entrez Gene ID:

 104355145

Gene Name:

 NCOA7 antisense RNA 1

Gene Aliases:

 -

Location:

 Chr.6:125797861-125818858 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NCOA7-AS1 NR_126386.1
AW444508.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv950505 Chr.6:125772255 - 125803354 on Build GRCh38 Duplication NCOA7 NCOA7-AS1

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More Information


Additional Information:

For this assay, SNP(s) [rs113458485] 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

Gene Ontology Categories:

Function(s) Process(es)


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