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See other PIEZO1 CNV Assays ›
Gene Symbol
PIEZO1
Assay Reference Genome
Location

Chr.16:88721394 on build GRCh38
Cytoband
16q24.3
Assay ID Hs00462120_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 9780

Gene Name:

 piezo type mechanosensitive ion channel component 1

Gene Aliases:

 DHS, FAM38A, LMPH3, Mib

Location:

 Chr.16:88715338-88785220 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 38 - Exon 39
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PIEZO1 NM_001142864.3 NP_001136336.2
AB161230.1 BAF03565.1
BC150271.1
BE066337.1
D87071.1 BAA13240.1
KC602455.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1063024 Chr.16:88707330 - 89238482 on Build GRCh38 Gain LOC339059 ZNF778 SLC22A31 LOC100129697 CDH15 LOC101927793 LOC107987238 LOC100289580 CTU2 ACSF3 LINC00304 GALNS MIR4722 PIEZO1 CDT1 LOC400558 TRAPPC2L APRT CBFA2T3 LOC105371409 PABPN1L
nsv471113 Chr.16:88650665 - 88764428 on Build GRCh38 Loss LOC339059 MIR4722 PIEZO1 RNF166 SNAI3-AS1 LOC100289580 CTU2 MVD SNAI3 CYBA
dgv3064n100 Chr.16:88683753 - 88846491 on Build GRCh38 Gain LOC339059 GALNS MIR4722 PIEZO1 RNF166 CDT1 LOC107987238 SNAI3-AS1 LOC100289580 CTU2 APRT SNAI3
nsv517643 Chr.16:88713767 - 88756339 on Build GRCh38 Loss LOC339059 MIR4722 PIEZO1 LOC100289580 CTU2
nsv1065973 Chr.16:88661146 - 88731220 on Build GRCh38 Loss MIR4722 PIEZO1 RNF166 SNAI3-AS1 LOC100289580 CTU2 MVD SNAI3
nsv833327 Chr.16:88667431 - 88757621 on Build GRCh38 Loss LOC339059 MIR4722 PIEZO1 RNF166 SNAI3-AS1 LOC100289580 CTU2 SNAI3
nsv1927 Chr.16:88712585 - 88743583 on Build GRCh38 Insertion LOC339059 MIR4722 PIEZO1 LOC100289580 CTU2
nsv482951 Chr.16:88633593 - 90228345 on Build GRCh38 Loss LOC339059 DEF8 LOC100129697 LOC101927793 LOC107987238 LOC100289580 TUBB8P7 VPS9D1-AS1 SPATA33 ACSF3 GAS8 LINC00304 URAHP DBNDD1 SNAI3-AS1 APRT PRDM7 FANCA MVD CHMP1A CYBA TUBB3 LOC107984817 DPEP1 LOC105371414 TRAPPC2L RPL13 LOC101927817 IL17C ZNF778 SLC22A31 CENPBD1 GAS8-AS1 SPATA2L AFG3L1P SNORD68 RNF166 SPG7 LOC100287036 LOC105371419 SNAI3 PABPN1L CPNE7 VPS9D1 CDH15 MC1R CTU2 FAM157C CDK10 ANKRD11 GALNS MIR4722 PIEZO1 SPIRE2 ZNF276 CDT1 LOC400558 TCF25 CBFA2T3 LOC105371409
nsv471114 Chr.16:88688461 - 88756339 on Build GRCh38 Gain LOC339059 MIR4722 PIEZO1 RNF166 LOC100289580 CTU2
nsv573673 Chr.16:88721265 - 88735362 on Build GRCh38 Loss PIEZO1 LOC100289580
nsv952070 Chr.16:88257295 - 88780192 on Build GRCh38 Deletion LOC339059 ZFPM1 ZC3H18-AS1 LOC107984862 LOC100289580 CTU2 MVD ZC3H18 CYBA MIR5189 ZNF469 MIR4722 PIEZO1 RNF166 SNAI3-AS1 SNAI3 IL17C
nsv1160442 Chr.16:88708161 - 88778524 on Build GRCh38 Deletion LOC339059 MIR4722 PIEZO1 LOC100289580 CTU2
dgv3065n100 Chr.16:88711587 - 88927172 on Build GRCh38 Gain LOC339059 LOC101927793 LOC107987238 LOC100289580 CTU2 GALNS MIR4722 PIEZO1 CDT1 TRAPPC2L APRT CBFA2T3 PABPN1L

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More Information


Additional Information:

For this assay, SNP(s) [rs78574543] 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 Non-exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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