Prmt8 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Prmt8
protein arginine N-methyltransferase 8
MGI:3043083

7 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Prmt8^{tm1d(EUCOMM)Wtsi}/Prmt8⁺ involves: C57BL/6N	abnormal cerebellum morphology	J:234033
Prmt8^{tm1d(EUCOMM)Wtsi}/Prmt8⁺ involves: C57BL/6N	limb grasping	J:234033
Prmt8^{tm1d(EUCOMM)Wtsi}/Prmt8^{tm1d(EUCOMM)Wtsi} involves: C57BL/6N	abnormal cerebellum morphology	J:234033
	abnormal gait	J:234033
	abnormal Purkinje cell dendrite morphology	J:234033
	abnormal response to new environment	J:234033
	decreased neurotransmitter release	J:234033
	hyperactivity	J:234033
	limb grasping	J:234033

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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