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 RBFOX1 CNV Assays ›
Gene Symbol
RBFOX1
Assay Reference Genome
Location

Chr.16:5312891 on build GRCh38
Cytoband
16p13.3
Assay ID Hs03940456_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 54715

Gene Name:

 RNA binding protein, fox-1 homolog 1

Gene Aliases:

 2BP1, A2BP1, FOX-1, FOX1, HRNBP1

Location:

 Chr.16:5239749-7713343 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RBFOX1 XM_017023319.1 XP_016878808.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1035156 Chr.16:5091032 - 5996934 on Build GRCh38 Gain MIR8065 EEF2KMT LINC01570 RBFOX1
nsv1046986 Chr.16:4049000 - 5555721 on Build GRCh38 Gain SEC14L5 C16orf96 SEPT12 GLIS2 NAGPA-AS1 ALG1 MIR6769A NMRAL1 C16orf71 MGRN1 GLYR1 ADCY9 UBALD1 EEF2KMT LOC105371063 PPL CORO7-PAM16 ANKS3 UBN1 DNAJA3 ROGDI CORO7 VASN NAGPA SMIM22 GLIS2-AS1 HMOX2 RBFOX1 NUDT16L1 PAM16 CDIP1 ZNF500 LINC01569 SRL C16orf89 TFAP4
nsv1045304 Chr.16:5205761 - 5326875 on Build GRCh38 Loss RBFOX1
esv34300 Chr.16:5005938 - 5322534 on Build GRCh38 Gain SEC14L5 NAGPA EEF2KMT RBFOX1 NAGPA-AS1 ALG1 C16orf89
nsv1036241 Chr.16:5271882 - 5387609 on Build GRCh38 Loss RBFOX1
dgv2698n100 Chr.16:5304641 - 5327717 on Build GRCh38 Loss RBFOX1
esv2760069 Chr.16:4922849 - 5374828 on Build GRCh38 Gain+Loss SEC14L5 NAGPA EEF2KMT PPL RBFOX1 NAGPA-AS1 ALG1 C16orf89
nsv428318 Chr.16:5011594 - 5374828 on Build GRCh38 Gain SEC14L5 NAGPA EEF2KMT RBFOX1 NAGPA-AS1 ALG1 C16orf89
nsv1037303 Chr.16:5287645 - 5327595 on Build GRCh38 Loss RBFOX1
esv2762021 Chr.16:5293419 - 5377238 on Build GRCh38 Loss RBFOX1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs75744218,rs78251475] 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