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Symbol
Name
ID

Inpp5e
inositol polyphosphate-5-phosphatase E
MGI:1927753

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes

Biparietal narrowing

Plagiocephaly

Microcephaly

Macrocephaly

Encephalocele

Long face

Prominent forehead

Macroglossia

Protruding tongue

Triangular-shaped open mouth

Orofacial cleft

Anteverted nares

Prominent nasal bridge

Highly arched eyebrow

Epicanthus

Disease(s) Associated with INPP5E

Joubert syndrome

Joubert syndrome 1

Mouse Phenotypes		abnormal craniofacial morphology	palatal shelves fail to meet at midline	palatal shelf hypoplasia	cleft palate
Availability	Mouse Genotype	abnormal craniofacial morphology	palatal shelves fail to meet at midline	palatal shelf hypoplasia	cleft palate
	Inpp5e^{tm1.1(KOMP)Vlcg}/Inpp5e^{tm1.1(KOMP)Vlcg}
	Inpp5e^tm1.2Ssch/Inpp5e^tm1.2Ssch

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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