PIEZO1 Chromosome 16

Piezo type mechanosensitive ion channel component 1 (Er blood group)
390 variants 390 Health Risk

Upload your DNA to see your personal genotypes for variants in PIEZO1.

What This Gene Does
The protein encoded by this gene is a mechanically-activated ion channel that links mechanical forces to biological signals. The encoded protein contains 36 transmembrane domains and functions as a homotetramer. Defects in this gene have been associated with dehydrated hereditary stomatocytosis. [provided by RefSeq, Jul 2015]
Gene Info
Gene Group
"Blood group antigens|MicroRNA protein coding host genes|Piezo type mechanosensitive ion channel components"
Locus Type
gene with protein product
Location
16q24.3
Ensembl
ENSG00000103335
Associated Conditions (20)
Inborn genetic diseases
Lymphatic malformation 6
Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema
PIEZO1-related disorder
Non-immune hydrops fetalis
Pancytopenia
Malignant tumor of esophagus
Familial cancer of breast
Blood group
ER
Hydrops fetalis
ER BLOOD GROUP SYSTEM
ER(a-b-)
Polyhydramnios
Thickened nuchal skin fold
Sarcoma
Ovarian serous cystadenocarcinoma
Thymoma
Cervical cancer
Diffuse lymphatic malformation
Key Variants
All Variants (390)
RSID Category Clinical Significance Conditions
RS771886999 Health Risk Conflicting classifications of pathogenicity
RS772788410 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema, Lymphatic malformation 6
RS773006843 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Lymphatic malformation 6, Inborn genetic diseases
RS773645030 Health Risk Conflicting classifications of pathogenicity
RS773795281 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Lymphatic malformation 6, Inborn genetic diseases
RS773860217 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774090082 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774583059 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774602954 Health Risk Conflicting classifications of pathogenicity
RS775326454 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PIEZO1-related disorder, Inborn genetic diseases
RS775331933 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS775384549 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS776396482 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS776531529 Health Risk Conflicting classifications of pathogenicity
RS776672249 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS776788949 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, PIEZO1-related disorder
RS776838552 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS777483750 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS777875339 Health Risk Conflicting classifications of pathogenicity
RS778144394 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778223284 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778289969 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778813372 Health Risk Conflicting classifications of pathogenicity Lymphatic malformation 6, Inborn genetic diseases, Lymphatic malformation 6
RS778920824 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Lymphatic malformation 6, Inborn genetic diseases
RS779186692 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS779308700 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS779772252 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, PIEZO1-related disorder
RS780025201 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Lymphatic malformation 6, Inborn genetic diseases
RS780260086 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS780275226 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS780831903 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS79879471 Health Risk Conflicting classifications of pathogenicity
RS8055062 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS866069095 Health Risk Conflicting classifications of pathogenicity
RS866681472 Health Risk Conflicting classifications of pathogenicity
RS868467734 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS868678918 Health Risk Conflicting classifications of pathogenicity
RS886041515 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS897963232 Health Risk Conflicting classifications of pathogenicity
RS902069811 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema, Inborn genetic diseases
RS907173644 Health Risk Conflicting classifications of pathogenicity
RS910772546 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS917988282 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases, Inborn genetic diseases
RS920924223 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS922432809 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Lymphatic malformation 6, Inborn genetic diseases
RS923513392 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS930735351 Health Risk Conflicting classifications of pathogenicity
RS942498680 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, PIEZO1-related disorder
RS946453254 Health Risk Conflicting classifications of pathogenicity PIEZO1-related disorder, PIEZO1-related disorder
RS947487272 Health Risk Conflicting classifications of pathogenicity Lymphatic malformation 6, Inborn genetic diseases, Lymphatic malformation 6
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