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

Chr.1:3878531 on build GRCh38
Cytoband
1p36.32
Assay ID Hs05791404_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 1677

Gene Name:

 DNA fragmentation factor subunit beta

Gene Aliases:

 CAD, CPAN, DFF-40, DFF2, DFF40

Location:

 Chr.1:3857143-3885429 on Build GRCh38

Assay Gene Location:

 Within Intron 9
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
DFFB NM_001282669.1 NP_001269598.1
NM_001320132.1 NP_001307061.1
NM_001320136.1 NP_001307065.1
NM_004402.3 NP_004393.1
NR_104222.1
NR_135150.1
NR_135151.1
NR_135152.1
XM_017000498.1 XP_016855987.1
XM_017000499.1 XP_016855988.1
XM_017000500.1 XP_016855989.1
AB013918.1 BAA32250.1
AB028911.1 BAB40447.1
AB028912.1 BAB40448.1
AB028913.1 BAB40449.1
AF039210.1 AAC39709.1
AF064019.1 AAC39920.1
AF409060.1 AAL02005.1
AF409061.1 AAL02006.1
AF409062.1 AAL02007.1
AK290877.1
AK303065.1
AY438267.1 AAR05821.1
AY438268.1 AAR05822.1
BC032827.1 AAH32827.1
BC048797.1 AAH48797.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3585042 Chr.1:3585575 - 4260083 on Build GRCh38 Gain WRAP73 DFFB C1orf174 TP73 CCDC27 MEGF6 TP73-AS1 SMIM1 CEP104 TPRG1L LRRC47 LINC01346 LINC01134
nsv1012423 Chr.1:3477686 - 4747449 on Build GRCh38 Gain AJAP1 LOC284661 WRAP73 ARHGEF16 DFFB C1orf174 TP73 CCDC27 MEGF6 TP73-AS1 SMIM1 CEP104 TPRG1L MIR551A LRRC47 LINC01346 LINC01134
nsv509590 Chr.1:3826457 - 3902492 on Build GRCh38 Insertion CEP104 DFFB C1orf174 LINC01134
esv3585052 Chr.1:3817921 - 3928224 on Build GRCh38 Gain CEP104 DFFB C1orf174 LINC01134
nsv545130 Chr.1:3826568 - 4283888 on Build GRCh38 Gain CEP104 DFFB LINC01346 C1orf174 LINC01134

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More Information


Additional Information:

For this assay, SNP(s) [rs72848499] 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)


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