This product has been added to your favorites list. Go to My Favorites

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

    

System Message

OKCancel
LOADING ...
  • Home
  • › Search Tool
  • › Search Results
  • › Hs03375204_cn
See other MEGF6 CNV Assays ›
Gene Symbol
MEGF6
Assay Reference Genome
Location

Chr.1:3491406 on build GRCh38
Cytoband
1p36.32
Assay ID Hs03375204_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›
  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

LOADING...
×
Back To Top

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 Intron 39
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MEGF6 NM_001409.3 NP_001400.3
XM_006710406.3 XP_006710469.1
XM_011540885.1 XP_011539187.1
XM_011540886.1 XP_011539188.1
XM_011540887.2 XP_011539189.1
XM_017000533.1 XP_016856022.1
AB011539.2 BAA32467.2
AB231860.1

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 TPRG1L WRAP73 ARHGEF16 MEGF6 PRDM16 MIR551A
nsv470687 Chr.1:3356499 - 3763210 on Build GRCh38 Loss TPRG1L WRAP73 ARHGEF16 TP73 CCDC27 TP73-AS1 MEGF6 PRDM16 MIR551A
nsv1012423 Chr.1:3477686 - 4747449 on Build GRCh38 Gain SMIM1 WRAP73 ARHGEF16 CEP104 LOC284661 TP73 LINC01134 LINC01346 MEGF6 LRRC47 C1orf174 TPRG1L AJAP1 CCDC27 TP73-AS1 DFFB MIR551A
nsv951959 Chr.1:3051037 - 3812036 on Build GRCh38 Deletion SMIM1 WRAP73 LOC105378604 ARHGEF16 TP73 LINC00982 MEGF6 LRRC47 PRDM16 TPRG1L CCDC27 TP73-AS1 MIR551A MIR4251
esv3893545 Chr.1:3460878 - 3512044 on Build GRCh38 Loss ARHGEF16 MEGF6
nsv545125 Chr.1:3490443 - 3540731 on Build GRCh38 Loss MEGF6
nsv830203 Chr.1:3446374 - 3607752 on Build GRCh38 Loss ARHGEF16 MEGF6 MIR551A
nsv299 Chr.1:3476928 - 3512705 on Build GRCh38 Insertion ARHGEF16 MEGF6

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs116356157] 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 -

extracellular matrix protein

Gene Ontology Categories:

Function(s) Process(es)

biological_process
calcium ion binding
protein binding

Back To Top

Related Products

  • TaqMan® Genotyping Master Mix
  • TaqPath®ProAmp® Master Mix
  • TaqMan® Universal Master Mix II, no UNG
  • TaqMan® Gene Expression Master Mix
  • TaqMan® Universal PCR Master Mix
  • TaqMan® Universal PCR Master Mix, No AmpErase UNG

Your items have has been added!


Host server : magellan-search-blue-7c59b9b899-zvjvc:80/100.66.72.70:80.
git-commit: 8ef7cf686e3c81d28b13492708ce56d167b2f995
git-url: https://github.com/thermofisher/magellan-search
git-branch: release/2.49.0-Offline