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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 PIEZO1 CDT1 CTU2 PABPN1L LOC101927793 GALNS LOC107987238 SLC22A31 LOC400558 LOC100289580 CBFA2T3 LOC105371409 LINC00304 LOC339059 ZNF778 CDH15 APRT ACSF3 MIR4722 TRAPPC2L LOC100129697
nsv471113 Chr.16:88650665 - 88764428 on Build GRCh38 Loss PIEZO1 CYBA CTU2 LOC100289580 MVD SNAI3-AS1 LOC339059 RNF166 MIR4722 SNAI3
dgv3064n100 Chr.16:88683753 - 88846491 on Build GRCh38 Gain PIEZO1 CDT1 CTU2 LOC100289580 GALNS LOC107987238 SNAI3-AS1 LOC339059 RNF166 APRT MIR4722 SNAI3
nsv1065973 Chr.16:88661146 - 88731220 on Build GRCh38 Loss PIEZO1 CTU2 LOC100289580 MVD SNAI3-AS1 RNF166 MIR4722 SNAI3
nsv517643 Chr.16:88713767 - 88756339 on Build GRCh38 Loss PIEZO1 CTU2 LOC100289580 LOC339059 MIR4722
nsv833327 Chr.16:88667431 - 88757621 on Build GRCh38 Loss PIEZO1 CTU2 LOC100289580 SNAI3-AS1 LOC339059 RNF166 MIR4722 SNAI3
nsv482951 Chr.16:88633593 - 90228345 on Build GRCh38 Loss PIEZO1 SPIRE2 LOC400558 CBFA2T3 TUBB3 RPL13 SNORD68 MC1R GAS8 SPATA33 VPS9D1-AS1 CDT1 CYBA LOC107984817 GALNS DEF8 CPNE7 AFG3L1P LOC105371419 SPG7 ZNF778 VPS9D1 GAS8-AS1 PABPN1L LOC101927793 LOC101927817 LOC107987238 FANCA CENPBD1 TCF25 DPEP1 DBNDD1 LOC100287036 LINC00304 RNF166 CDH15 APRT CDK10 ACSF3 IL17C SPATA2L CTU2 MVD PRDM7 ANKRD11 TUBB8P7 SLC22A31 LOC105371414 CHMP1A LOC100289580 URAHP LOC105371409 FAM157C SNAI3-AS1 LOC339059 MIR4722 TRAPPC2L SNAI3 ZNF276 LOC100129697
nsv1927 Chr.16:88712585 - 88743583 on Build GRCh38 Insertion PIEZO1 CTU2 LOC100289580 LOC339059 MIR4722
nsv471114 Chr.16:88688461 - 88756339 on Build GRCh38 Gain PIEZO1 CTU2 LOC100289580 LOC339059 RNF166 MIR4722
nsv573673 Chr.16:88721265 - 88735362 on Build GRCh38 Loss PIEZO1 LOC100289580
nsv952070 Chr.16:88257295 - 88780192 on Build GRCh38 Deletion PIEZO1 CYBA CTU2 MVD ZNF469 LOC107984862 ZC3H18 ZC3H18-AS1 LOC100289580 ZFPM1 SNAI3-AS1 LOC339059 RNF166 MIR5189 IL17C MIR4722 SNAI3
nsv1160442 Chr.16:88708161 - 88778524 on Build GRCh38 Deletion PIEZO1 CTU2 LOC100289580 LOC339059 MIR4722
nsv1061256 Chr.16:88711587 - 89013365 on Build GRCh38 Gain PIEZO1 CDT1 CTU2 PABPN1L LOC101927793 GALNS LOC107987238 LOC100289580 CBFA2T3 LOC105371409 LOC339059 APRT MIR4722 TRAPPC2L LOC100129697

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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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