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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ccn3
cellular communication network factor 3
MGI:109185
53 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ccn3em1(IMPC)Mbp/Ccn3em1(IMPC)Mbp
C57BL/6N-Ccn3em1(IMPC)Mbp/MbpMmucd 		abnormal heart morphology J:211773
abnormal kidney morphology J:211773
abnormal liver morphology J:211773
abnormal spleen morphology J:211773
abnormal vitreous body morphology J:211773
anophthalmia J:211773
blind uterus J:211773
enlarged heart J:211773
enlarged kidney J:211773
enlarged spleen J:211773
small spleen J:211773
Ccn3tm1.1Ecan/Ccn3tm1.1Ecan
B6.Cg-Ccn3tm1.1Ecan 		abnormal bone ossification J:158478
abnormal osteoblast physiology J:158478
abnormal osteoclast differentiation J:158478
abnormal osteoclast physiology J:158478
abnormal skeleton morphology J:158478
abnormal skeleton physiology J:158478
normal adipose tissue phenotype J:158478
decreased bone trabecula number J:158478
decreased bone volume J:158478
normal growth/size/body region phenotype J:158478
increased compact bone thickness J:158478
long femur J:158478
normal skeleton phenotype J:158478
Ccn3tm1Cabo/Ccn3+
involves: 129S/SvEv 		abnormal bone ossification J:135676
abnormal bone structure J:135676
abnormal carpal bone morphology J:135676
abnormal cartilage development J:135676
abnormal caudal vertebrae morphology J:135676
abnormal chondrocyte morphology J:135676
abnormal interventricular septum morphology J:135676
abnormal joint mobility J:135676
abnormal patella morphology J:135676
abnormal skeleton morphology J:135676
barrel chest J:135676
cataract J:135676
decreased survivor rate J:135676
delayed endochondral bone ossification J:135676
dystrophic cardiac calcinosis J:135676
embryonic lethality, incomplete penetrance J:135676
enlarged cranium J:135676
fused tarsal bones J:135676
hip dislocation J:135676
increased length of long bones J:135676
kidney vascular congestion J:135676
kinked tail J:135676
limp posture J:135676
liver vascular congestion J:135676
venoocclusion J:135676
ventricular cardiomyopathy J:135676
Ccn3tm1Cabo/Ccn3tm1Cabo
involves: 129S/SvEv 		abnormal body wall morphology J:135676
abnormal bone ossification J:135676
abnormal bone structure J:135676
abnormal carpal bone morphology J:135676
abnormal cartilage development J:135676
abnormal caudal vertebrae morphology J:135676
abnormal chondrocyte morphology J:135676
abnormal interventricular septum morphology J:135676
abnormal joint mobility J:135676
abnormal patella morphology J:135676
abnormal skeleton morphology J:135676
barrel chest J:135676
cataract J:135676
decreased survivor rate J:135676
delayed endochondral bone ossification J:135676
dystrophic cardiac calcinosis J:135676
embryonic lethality, incomplete penetrance J:135676
enlarged cranium J:135676
fused tarsal bones J:135676
hip dislocation J:135676
increased atrioventricular cushion size J:135676
increased length of long bones J:135676
kidney vascular congestion J:135676
kinked tail J:135676
limp posture J:135676
liver vascular congestion J:135676
muscular atrophy J:135676
venoocclusion J:135676
ventricular cardiomyopathy J:135676
Ccn3tm1Hko/Ccn3tm1Hko
B6.129-Ccn3tm1Hko 		abnormal vascular wound healing J:172144
increased vascular smooth muscle cell proliferation J:172144
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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Send questions and comments to User Support. 		last database update
06/12/2024
MGI 6.13 		The Jackson Laboratory