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Symbol
Name
ID
Porcn
porcupine O-acyltransferase
MGI:1890212
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Hydrocephalus
Agenesis of corpus callosum
Chiari malformation
Myelomeningocele
Spina bifida
Spina bifida occulta
Cognitive impairment
Intellectual disability
Disease(s) Associated with PORCN
focal dermal hypoplasia

Mouse Phenotypes
nervous system phenotype
open neural tube
abnormal midbrain-hindbrain boundary morphology
Availability Mouse Genotype
Porcntm1.2Lcm/Porcntm1.2Lcm
Porcntm1.1Lcm/Porcntm1.2Lcm
Porcntm1.1Lcm/Y
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)
Porcntm1.1Lcm/Y
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(rx3-icre)1Mjam/0  (conditional)
Porcntm1.1Vdv/Porcn+
Hprt1tm1(CAG-cre)Mnn/Hprt1+  (conditional)
Porcntm1.1Jrt/Porcn+
Tg(CAG-cre)1Nagy/0  (conditional)
*
Porcntm1.1Lcm/Porcntm1.2Lcm
Tg(Six3-cre)69Frty/0  (conditional)
Porcntm1.1Lcm/Y
Tg(rx3-icre)1Mjam/0  (conditional)

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
04/23/2024
MGI 6.23
The Jackson Laboratory