Symbol Name ID |
Nus1
NUS1 dehydrodolichyl diphosphate synthase subunit MGI:1196365 |
Darker colors indicate more annotations |
Human Phenotypes | Attenuation of retinal blood vessels |
Disease(s) Associated with NUS1 | |
congenital disorder of glycosylation Iaa |
Mouse Phenotypes | abnormal brain vasculature morphology |
abnormal placenta vasculature |
abnormal vascular development |
abnormal vitelline vasculature morphology |
hemorrhage |
abnormal vascular endothelial cell physiology |
increased vascular endothelial cell apoptosis |
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Availability | Mouse Genotype | |||||||
Nus1tm1.2Qrm/Nus1+ | ||||||||
Nus1tm1.1Qrm/Nus1tm1.1Qrm Tg(Tek-cre)1Ywa/0 (conditional) |
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Nus1tm1.1Qrm/Nus1tm1.1Qrm Tg(Cdh5-cre/ERT2)1Rha/0 (conditional) |
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Nus1tm1Wcsa/Nus1tm1Wcsa Tg(Tek-cre)12Flv/0 (conditional) |
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Nus1tm1Wcsa/Nus1tm1Wcsa Tg(Cdh5-cre/ERT2)1Rha/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 04/30/2024 MGI 6.23 |
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