Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other MEGF6 CNV Assays ›
Gene Symbol
MEGF6
Assay Reference Genome
Location

Chr.1:3489931 on build GRCh38
Cytoband
1p36.32
Assay ID Hs00290709_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 1953

Gene Name:

 multiple EGF like domains 6

Gene Aliases:

 EGFL3

Location:

 Chr.1:3487942-3624757 on Build GRCh38

Assay Gene Location:

 Within Exon 41
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MEGF6 NM_001409.3 37 5450 NP_001400.3
XM_006710406.3 34 5085 XP_006710469.1
XM_011540885.1 38 5755 XP_011539187.1
XM_011540886.1 37 5626 XP_011539188.1
XM_011540887.2 33 4963 XP_011539189.1
XM_017000533.1 37 5623 XP_016856022.1
AB011539.2 BAA32467.2
AB231860.1
AF086226.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2758915 Chr.1:3372374 - 3632289 on Build GRCh38 Gain ARHGEF16 PRDM16 TPRG1L MIR551A MEGF6 WRAP73
nsv470687 Chr.1:3356499 - 3763210 on Build GRCh38 Loss TP73-AS1 ARHGEF16 PRDM16 TPRG1L TP73 MIR551A CCDC27 MEGF6 WRAP73
nsv1012423 Chr.1:3477686 - 4747449 on Build GRCh38 Gain C1orf174 LINC01134 SMIM1 ARHGEF16 CEP104 TPRG1L LRRC47 LOC284661 MIR551A CCDC27 AJAP1 MEGF6 TP73-AS1 LINC01346 TP73 DFFB WRAP73
nsv951959 Chr.1:3051037 - 3812036 on Build GRCh38 Deletion SMIM1 ARHGEF16 LOC105378604 PRDM16 TPRG1L LRRC47 MIR551A CCDC27 LINC00982 MEGF6 TP73-AS1 MIR4251 TP73 WRAP73
esv3893545 Chr.1:3460878 - 3512044 on Build GRCh38 Loss ARHGEF16 MEGF6
nsv830203 Chr.1:3446374 - 3607752 on Build GRCh38 Loss ARHGEF16 MIR551A MEGF6
nsv299 Chr.1:3476928 - 3512705 on Build GRCh38 Insertion ARHGEF16 MEGF6

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs74636253] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

extracellular matrix protein

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products