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See other HES2 CNV Assays ›
Gene Symbol
HES2
Assay Reference Genome
Location

Chr.1:6416487 on build GRCh38
Cytoband
1p36.31
Assay ID Hs02408917_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

54626

Gene Name:

hes family bHLH transcription factor 2

Gene Aliases:

bHLHb40

Location:

Chr.1:6415232-6419919 on Build GRCh38

Assay Gene Location:

Within Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HES2 NM_019089.4 4 3007 NP_061962.2
AK023754.1 1 2192
AK091122.1 4 3007
BC012091.1 AAH12091.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv1009548 Chr.1:6342976 - 6517352 on Build GRCh38 Loss ACOT7 PLEKHG5 HES2 MIR4252 TNFRSF25 ESPN
dgv2n27 Chr.1:6396412 - 6512115 on Build GRCh38 Loss PLEKHG5 HES2 MIR4252 TNFRSF25 ESPN
nsv954048 Chr.1:6414241 - 6500740 on Build GRCh38 Deletion PLEKHG5 HES2 MIR4252 TNFRSF25 ESPN
nsv545240 Chr.1:6351154 - 6512115 on Build GRCh38 Loss ACOT7 PLEKHG5 HES2 MIR4252 TNFRSF25 ESPN
nsv508836 Chr.1:6406896 - 6501029 on Build GRCh38 Insertion PLEKHG5 HES2 MIR4252 TNFRSF25 ESPN

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More Information


Additional Information:

For this assay, SNP(s) [rs78326109] 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 -

basic helix-loop-helix transcription factor

Gene Ontology Categories:

Function(s) Process(es)

transcription, DNA-templated
negative regulation of transcription, DNA-templated
double-stranded DNA binding
transcription factor binding
protein dimerization activity

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