Symbol Name ID |
Piezo1
piezo-type mechanosensitive ion channel component 1 MGI:3603204 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Disease(s) Associated with PIEZO1 | |
dehydrated hereditary stomatocytosis 1 |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal vascular endothelial cell morphology |
abnormal intersomitic vessel morphology |
abnormal developmental vascular remodeling |
absent organized vascular network |
abnormal vitelline vasculature morphology |
disorganized yolk sac vascular plexus |
pericardial effusion |
abnormal vascular endothelial cell physiology |
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Availability | Mouse Genotype | |||||||||
Piezo1Gt(RST343)Byg/Piezo1Gt(RST343)Byg | * | |||||||||
Piezo1tm1a(KOMP)Wtsi/Piezo1tm1a(KOMP)Wtsi | ||||||||||
Piezo1tm1a(KOMP)Wtsi/Piezo1+ | ||||||||||
Piezo1tm1c(KOMP)Wtsi/Piezo1tm1c(KOMP)Wtsi Tg(Tek-cre)12Flv/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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