Cnp Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cnp
2',3'-cyclic nucleotide 3' phosphodiesterase
MGI:88437

15 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cnp^tm1(cre)Kan/Cnp^tm1(cre)Kan B6N.129-Cnp^tm1(cre)Kan	axon degeneration	J:236408
	dysmyelination	J:236408
	tomacula	J:236408
Cnp^tm1(cre)Kan/Cnp^tm1(cre)Kan involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal gait	J:91814
	ataxia	J:91814
	axon degeneration	J:91814
	convulsive seizures	J:91814
	gliosis	J:91814
	hindlimb paralysis	J:91814
	kyphosis	J:91814
	muscle weakness	J:91814
	premature death	J:91814
	weight loss	J:91814
Cnp^{tm1b(EUCOMM)Wtsi}/Cnp^{tm1b(EUCOMM)Wtsi} C57BL/6N-Cnp^{tm1b(EUCOMM)Wtsi}/H	abnormal behavior	J:211773
	decreased locomotor activity	J:211773
	decreased thigmotaxis	J:211773

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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