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Symbol
Name
ID

Pign
phosphatidylinositol glycan anchor biosynthesis, class N
MGI:1351629

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Spasticity	Cerebral atrophy	Cerebellar atrophy	Choreoathetosis	Tremor	Absent speech	Intellectual disability	Hyperreflexia	Hyporeflexia	Global developmental delay	Seizure
Disease(s) Associated with PIGN
multiple congenital anomalies-hypotonia-seizures syndrome 1

Mouse Phenotypes		abnormal forebrain development	holoprosencephaly	forebrain hypoplasia	midbrain hypoplasia	exencephaly
Availability	Mouse Genotype	abnormal forebrain development	holoprosencephaly	forebrain hypoplasia	midbrain hypoplasia	exencephaly
	Pign^em1(IMPC)Mbp/Pign^em1(IMPC)Mbp
	Pign^m1Nisw/Pign^m1Nisw

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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