Symbol Name ID |
Pign
phosphatidylinositol glycan anchor biosynthesis, class N MGI:1351629 |
Darker colors indicate more annotations |
Human Phenotypes | Polyhydramnios |
Disease(s) Associated with PIGN | |
multiple congenital anomalies-hypotonia-seizures syndrome 1 |
Mouse Phenotypes | abnormal anterior visceral endoderm cell migration |
abnormal gastrulation |
embryonic growth retardation |
abnormal anterior definitive endoderm morphology |
abnormal anterior visceral endoderm morphology |
abnormal distal visceral endoderm morphology |
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Availability | Mouse Genotype | ||||||
Pignem1(IMPC)Mbp/Pignem1(IMPC)Mbp | |||||||
Pignm1Nisw/Pignm1Nisw | |||||||
Pignm1Nisw/Pignm1Nisw Tg(Hhex-EGFP)#Rbe/0 |
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 04/16/2024 MGI 6.23 |
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