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Symbol
Name
ID
Pign
phosphatidylinositol glycan anchor biosynthesis, class N
MGI:1351629
Phenotype annotations related to embryo
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
Availability Mouse Genotype
Pignem1(IMPC)Mbp/Pignem1(IMPC)Mbp
Pignm1Nisw/Pignm1Nisw
Pignm1Nisw/Pignm1Nisw
Tg(Hhex-EGFP)#Rbe/0

Contributing Projects:
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
The Jackson Laboratory