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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pde4dip
phosphodiesterase 4D interacting protein (myomegalin)
MGI:1891434
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Pde4diptm1b(KOMP)Wtsi/Pde4dip+
C57BL/6N-Pde4diptm1b(KOMP)Wtsi/Bay 		abnormal eye anterior chamber depth J:211773
abnormal retina outer nuclear layer morphology J:211773
decreased total retina thickness J:211773
increased bone mineral content J:211773
increased cornea thickness J:211773
increased hemoglobin content J:211773
Pde4diptm1b(KOMP)Wtsi/Pde4diptm1b(KOMP)Wtsi
C57BL/6N-Pde4diptm1b(KOMP)Wtsi/Bay 		preweaning lethality, complete penetrance J:211773
Pde4diptm1Mhda/Pde4diptm1Mhda
B6.Cg-Pde4diptm1Mhda 		normal behavior/neurological phenotype J:216968
normal growth/size/body region phenotype J:216968
hyperactivity J:216968
increased vertical activity J:216968
lethality, incomplete penetrance J:216968
normal nervous system phenotype J:216968
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
11/12/2024
MGI 6.24 		The Jackson Laboratory