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Symbol
Name
ID
Pign
phosphatidylinositol glycan anchor biosynthesis, class N
MGI:1351629
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Congenital diaphragmatic hernia
Large for gestational age
Disease(s) Associated with PIGN
multiple congenital anomalies-hypotonia-seizures syndrome 1

Mouse Phenotypes
facial cleft
abnormal head shape
proboscis
embryonic growth retardation
decreased fetal size
enlarged spleen
Availability Mouse Genotype
Pignem1(IMPC)Mbp/Pignem1(IMPC)Mbp
Pignm1Nisw/Pignm1Nisw
Pignem1(IMPC)Mbp/Pign+

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