accessibility menu, dialog, popup

UserName
Viewing profile as user:

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

    

System Message

OKCancel
LOADING ...
See other ARHGEF4 CNV Assays ›
Gene Symbol
ARHGEF4
Assay Reference Genome
Location

Chr.2:130847830 on build GRCh38
Cytoband
2q21.1
Assay ID Hs03431718_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 50649

Gene Name:

 Rho guanine nucleotide exchange factor 4

Gene Aliases:

 ASEF, ASEF1, GEF4, STM6

Location:

 Chr.2:130836916-131047253 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ARHGEF4 XM_005263681.1 XP_005263738.1
XM_005263685.3 XP_005263742.1
XM_011511274.2 XP_011509576.1
XM_017004231.1 XP_016859720.1
AK127124.1

Target Gene Details

Entrez Gene ID:

 653269

Gene Name:

 POTE ankyrin domain family member I

Gene Aliases:

 POTE2beta

Location:

 Chr.2:130462245-131626428 on Build GRCh38

Assay Gene Location:
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
POTEI

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv4074n100 Chr.2:130550793 - 131291209 on Build GRCh38 Gain FAM168B AMER3 LOC440910 CYP4F30P POTEI CFC1 GPR148 POTEJ PLEKHB2 TISP43 ARHGEF4 POTEE
dgv731e199 Chr.2:130678437 - 131300107 on Build GRCh38 Deletion FAM168B AMER3 LOC440910 CYP4F30P POTEI GPR148 PLEKHB2 ARHGEF4 POTEE
esv2670824 Chr.2:130625264 - 131605218 on Build GRCh38 Deletion FAM168B MIR4784 CCDC74A LOC150776 NOC2LP2 CYP4F30P GPR148 POTEJ ARHGEF4 LINC01120 TUBA3D WTH3DI POTEKP AMER3 LOC440910 MZT2A POTEI PLEKHB2 POTEE
dgv4075n100 Chr.2:130720375 - 131521740 on Build GRCh38 Gain FAM168B MIR4784 LOC150776 NOC2LP2 GPR148 ARHGEF4 LINC01120 TUBA3D WTH3DI AMER3 LOC440910 MZT2A POTEI PLEKHB2 POTEE
nsv2925 Chr.2:130841107 - 130887218 on Build GRCh38 Deletion POTEI ARHGEF4
nsv517274 Chr.2:130845653 - 130865593 on Build GRCh38 Loss POTEI ARHGEF4
esv3893337 Chr.2:130722838 - 131194387 on Build GRCh38 Loss FAM168B AMER3 POTEI GPR148 PLEKHB2 ARHGEF4
dgv616e201 Chr.2:130674635 - 131312550 on Build GRCh38 Deletion FAM168B AMER3 LOC440910 CYP4F30P POTEI GPR148 PLEKHB2 ARHGEF4 POTEE
nsv583135 Chr.2:130724905 - 131194388 on Build GRCh38 Loss FAM168B AMER3 POTEI GPR148 PLEKHB2 ARHGEF4
nsv524021 Chr.2:130724906 - 131553515 on Build GRCh38 Loss FAM168B MIR4784 CCDC74A LOC150776 NOC2LP2 GPR148 ARHGEF4 LINC01120 TUBA3D WTH3DI AMER3 LOC440910 MZT2A POTEI PLEKHB2 POTEE
esv2760576 Chr.2:130634172 - 131521752 on Build GRCh38 Gain+Loss FAM168B MIR4784 LOC150776 NOC2LP2 CYP4F30P GPR148 POTEJ ARHGEF4 LINC01120 TUBA3D WTH3DI AMER3 LOC440910 MZT2A POTEI PLEKHB2 POTEE
esv2759092 Chr.2:129589265 - 132440430 on Build GRCh38 Gain+Loss NOC2LP2 GPR148 MED15P9 FAM201B ARHGEF4 LOC107985778 TUBA3D MIR663B LOC440910 MZT2A POTEF ZNF806 PLEKHB2 POTEE RAB6C CCDC115 CFC1 POTEJ LINC01120 LINC01087 TUBA3E PTPN18 SMPD4 FAM168B MIR4784 LOC100507460 LOC150776 ANKRD30BL CFC1B IMP4 RAB6C-AS1 LOC389033 POTEKP GPR39 MZT2B FAR2P1 TISP43 NOC2LP1 CCDC74A CYP4F30P FAR2P2 CYP4F62P CCDC74B WTH3DI AMER3 C2orf27B LOC101927924 POTEI LOC646743 C2orf27A
nsv523500 Chr.2:130835472 - 130853759 on Build GRCh38 Loss POTEI ARHGEF4
nsv428403 Chr.2:129818076 - 130882067 on Build GRCh38 Loss SMPD4 CFC1B GPR148 IMP4 MED15P9 ARHGEF4 LOC107985778 RAB6C-AS1 LOC389033 MZT2B POTEF FAR2P1 TISP43 NOC2LP1 RAB6C CCDC115 CYP4F30P FAR2P2 CYP4F62P CFC1 POTEJ CCDC74B AMER3 TUBA3E LOC101927924 POTEI LOC646743 PTPN18

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs113448370] 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:

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products