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See other ABHD14A CNV Assays ›
Gene Symbol
ABHD14A
Assay Reference Genome
Location

Chr.3:51980992 on build GRCh38
Cytoband
3p21.2
Assay ID Hs01526356_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 25864

Gene Name:

 abhydrolase domain containing 14A

Gene Aliases:

 DORZ1

Location:

 Chr.3:51975026-51981200 on Build GRCh38

Assay Gene Location:

 Within Exon 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ABHD14A NM_015407.4 5 900 NP_056222.2
AL050015.1 5 811 CAB43237.2
AY358201.1 5 857 AAQ88568.1
BC002571.2 5 858 AAH02571.1
BM665207.1 1 226

Target Gene Details

Entrez Gene ID:

 100526760

Gene Name:

 ABHD14A-ACY1 readthrough

Gene Aliases:

 -

Location:

 Chr.3:51975026-51989202 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ABHD14A-ACY1 NM_001316331.1 NP_001303260.1
AK294015.1
AK298086.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1003453 Chr.3:51928065 - 52065425 on Build GRCh38 Gain ABHD14B PARP3 GPR62 DUSP7 RPL29 ABHD14A ACY1 ABHD14A-ACY1 LINC00696 RRP9 PCBP4
nsv508922 Chr.3:51940932 - 52009520 on Build GRCh38 Insertion ABHD14B PARP3 GPR62 RPL29 ABHD14A ACY1 ABHD14A-ACY1 RRP9 PCBP4
nsv954857 Chr.3:51932485 - 52056584 on Build GRCh38 Deletion ABHD14B PARP3 GPR62 DUSP7 RPL29 ABHD14A ACY1 ABHD14A-ACY1 RRP9 PCBP4
nsv519445 Chr.3:51970301 - 52333916 on Build GRCh38 Gain+Loss DNAH1 ABHD14B GLYCTK GLYCTK-AS1 PPM1M MIRLET7G TLR9 ALAS1 LINC00696 WDR82 MIR135A1 DUSP7 RPL29 ABHD14A TWF2 ACY1 LOC101929054 ABHD14A-ACY1 POC1A
nsv520211 Chr.3:51738331 - 52132131 on Build GRCh38 Gain IQCF5-AS1 ABHD14B PARP3 GPR62 IQCF5 LINC00696 RRP9 IQCF2 DUSP7 IQCF3 RPL29 ABHD14A IQCF1 IQCF6 ACY1 ABHD14A-ACY1 POC1A IQCF4 PCBP4

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More Information


Additional Information:

For this assay, SNP(s) [rs573368825] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Process(es)


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