P3h2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

P3h2
prolyl 3-hydroxylase 2
MGI:2146663

9 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
P3h2^em1(IMPC)H/P3h2⁺ C57BL/6N-P3h2^em1(IMPC)H/H	abnormal snout morphology	J:211773
P3h2^em1(IMPC)H/P3h2^em1(IMPC)H C57BL/6N-P3h2^em1(IMPC)H/H	decreased circulating fructosamine level	J:211773
	decreased locomotor activity	J:211773
	increased circulating potassium level	J:211773
P3h2^{tm1d(KOMP)Wtsi}/P3h2^{tm1d(KOMP)Wtsi} involves: C57BL/6J * C57BL/6N	abnormal eye physiology	J:220554
	normal skeleton phenotype	J:220554
P3h2^tm1Hpb/P3h2^tm1Hpb involves: 129 * C57BL/6J	abnormal thrombosis	J:206377
	embryonic lethality during organogenesis, complete penetrance	J:206377
	embryonic lethality, incomplete penetrance	J:206377

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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