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

Chr.10:86970822 on build GRCh38
Cytoband
10q23.2
Assay ID Hs02521464_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 10974

Gene Name:

 adipogenesis regulatory factor

Gene Aliases:

 AFRO, APM2, C10orf116, apM-2

Location:

 Chr.10:86968431-86970909 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ADIRF NM_006829.2 3 585 NP_006820.1
BM850559.1
CD722742.1 1 195

Target Gene Details

Entrez Gene ID:

 119385

Gene Name:

 ArfGAP with GTPase domain, ankyrin repeat and PH domain 11

Gene Aliases:

 -

Location:

 Chr.10:86970741-87010203 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
AGAP11 NM_133447.1 1 82 NP_597704.1
AK097165.1 1 82

Target Gene Details

Entrez Gene ID:

 79812

Gene Name:

 multimerin 2

Gene Aliases:

 EMILIN-3, EMILIN3, ENDOGLYX-1

Location:

 Chr.10:86935540-86971311 on Build GRCh38

Assay Gene Location:

 Within Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MMRN2 XM_006717970.3 1 490 XP_006718033.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv428236 Chr.10:86866859 - 87550005 on Build GRCh38 Loss SNCG FAM35A LINC00864 ADIRF MINPP1 NUTM2D NUTM2A BMPR1A MIR4678 NUTM2A-AS1 FAM25A GLUD1 LINC00863 MMRN2 AGAP11
nsv517487 Chr.10:86899290 - 86973435 on Build GRCh38 Gain+Loss SNCG BMPR1A ADIRF MMRN2 AGAP11
esv2759774 Chr.10:86755301 - 87550005 on Build GRCh38 Gain+Loss SNCG FAM35A LINC00864 ADIRF MINPP1 NUTM2D NUTM2A BMPR1A MIR4678 NUTM2A-AS1 FAM25A GLUD1 LINC00863 MMRN2 AGAP11
nsv470969 Chr.10:86936624 - 86972907 on Build GRCh38 Loss SNCG ADIRF MMRN2 AGAP11

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More Information


Additional Information:

For this assay, SNP(s) [rs73334941] 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

Gene Ontology Categories:

Function(s) Process(es)


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