Symbol
Name
ID

Pign
phosphatidylinositol glycan anchor biosynthesis, class N
MGI:1351629

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes

Frontal bossing

Micrognathia

Macrocephaly

Coarse facial features

Narrow forehead

Long philtrum

Thin vermilion border

Cleft palate

High palate

Open mouth

Anteverted nares

Depressed nasal bridge

Short nose

Epicanthus

Disease(s) Associated with PIGN

multiple congenital anomalies-hypotonia-seizures syndrome 1

Mouse Phenotypes		abnormal craniofacial morphology	abnormal cranium morphology	abnormal cranial cartilage morphology	abnormal interparietal bone morphology	small interparietal bone	abnormal occipital bone morphology	abnormal supraoccipital bone morphology	facial cleft	abnormal head shape	proboscis
Availability	Mouse Genotype	abnormal craniofacial morphology	abnormal cranium morphology	abnormal cranial cartilage morphology	abnormal interparietal bone morphology	small interparietal bone	abnormal occipital bone morphology	abnormal supraoccipital bone morphology	facial cleft	abnormal head shape	proboscis
	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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