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See other ATP6V0A4 CNV Assays ›
Gene Symbol
ATP6V0A4
Assay Reference Genome
Location

Chr.7:138707896 on build GRCh38
Cytoband
7q34
Assay ID Hs05020454_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 50617

Gene Name:

 ATPase H+ transporting V0 subunit a4

Gene Aliases:

 A4, ATP6N1B, ATP6N2, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2

Location:

 Chr.7:138706294-138799839 on Build GRCh38

Assay Gene Location:

 Within Intron 23
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ATP6V0A4 NM_020632.2 NP_065683.2
NM_130840.2 NP_570855.2
NM_130841.2 NP_570856.2
XM_005250393.1 XP_005250450.1
XM_005250394.3 XP_005250451.1
AF245517.1 AAG11415.1
AK055789.1 BAB71014.1
AK292945.1
BC109304.1 AAI09305.1
BC109305.1 AAI09306.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2735212 Chr.7:138060002 - 140415947 on Build GRCh38 Deletion JHDM1D-AS1 TRIM24 TMEM213 UBN2 AKR1D1 KLRG2 PARP12 ATP6V0A4 SVOPL RAB19 KIAA1549 CLEC2L TBXAS1 KDM7A FMC1 ZC3HAV1 LOC100129148 LOC105375532 TTC26 C7orf55-LUC7L2 HIPK2 SLC37A3 LOC105375531 MIR4468 LUC7L2 ZC3HAV1L
nsv1030956 Chr.7:138478424 - 138894773 on Build GRCh38 Gain ATP6V0A4 SVOPL TRIM24 KIAA1549 TMEM213

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More Information


Additional Information:

For this assay, SNP(s) [rs73166922] 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:

Molecular Function -

ATP synthase

Gene Ontology Categories:

Function(s) Process(es)


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