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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pcnt
pericentrin (kendrin)
MGI:102722
58 phenotypes from 4 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Pcntem1(IMPC)Mbp/Pcnt+
C57BL/6NCrl-Pcntem1(IMPC)Mbp/MbpMmucd 		abnormal eye morphology J:211773
abnormal kidney morphology J:211773
abnormal skin morphology J:211773
abnormal testis morphology J:211773
abnormal vitreous body morphology J:211773
anophthalmia J:211773
cataract J:211773
decreased body length J:211773
persistence of hyaloid vascular system J:211773
small kidney J:211773
small testis J:211773
Pcntem1(IMPC)Mbp/Pcntem1(IMPC)Mbp
C57BL/6NCrl-Pcntem1(IMPC)Mbp/MbpMmucd 		embryonic growth retardation J:211773
microphthalmia J:211773
preweaning lethality, complete penetrance J:211773
PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
B6.129P2-PcntGt(RRU388)Byg 		abnormal brain development J:226309
abnormal cortical ventricular zone morphology J:226309
abnormal craniofacial development J:226309
abnormal embryonic neuroepithelium morphology J:226309
abnormal eye morphology J:226309
abnormal head shape J:226309
abnormal heart morphology J:226309
abnormal heart septum morphology J:226309
abnormal hippocampus morphology J:226309
abnormal kidney morphology J:226309
abnormal mitotic spindle morphology J:226309
abnormal neuron differentiation J:226309
abnormal vascular development J:226309
anophthalmia J:226309
aortic valve regurgitation J:226309
atelectasis J:226309
atrial septal defect J:226309
atrioventricular septal defect J:226309
cleft palate J:226309
congestive heart failure J:226309
decreased brain size J:226309
decreased surfactant secretion J:226309
duplex kidney J:226309
enlarged brain ventricles J:226309
hemorrhage J:226309
hydrops fetalis J:226309
increased heart ventricle size J:226309
intracranial hemorrhage J:226309
kidney cortex cyst J:226309
kidney cyst J:226309
lethality throughout fetal growth and development, complete penetrance J:226309
microcephaly J:226309
microphthalmia J:226309
misaligned sternebrae J:226309
mitral valve regurgitation J:226309
overriding aortic valve J:226309
polydactyly J:226309
prenatal growth retardation J:226309
pulmonary hypoplasia J:226309
renal glomerulus cyst J:226309
syndactyly J:226309
thin cerebral cortex J:226309
thin cortical plate J:226309
ventricular septal defect J:226309
Pcntm239Asp/Pcnt+
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		premature death J:136795
sporadic seizures J:136795
Pcntm239Asp/Pcntm239Asp
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		abnormal cerebral cortex morphology J:136795
polydactyly J:136795
Pcntm275Asp/Pcnt+
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		premature death J:136795
sporadic seizures J:136795
Pcntm275Asp/Pcntm275Asp
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		abnormal cerebral cortex morphology J:136795
perinatal lethality J:136795
polydactyly J:136795
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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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory