Symbol Name ID |
P3h2
prolyl 3-hydroxylase 2 MGI:2146663 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
P3h2em1(IMPC)H/P3h2+ C57BL/6N-P3h2em1(IMPC)H/H |
abnormal snout morphology | J:211773 |
P3h2em1(IMPC)H/P3h2em1(IMPC)H C57BL/6N-P3h2em1(IMPC)H/H |
decreased circulating fructosamine level | J:211773 |
decreased locomotor activity | J:211773 | |
increased circulating potassium level | J:211773 | |
P3h2tm1d(KOMP)Wtsi/P3h2tm1d(KOMP)Wtsi involves: C57BL/6J * C57BL/6N |
abnormal eye physiology | J:220554 |
normal skeleton phenotype | J:220554 | |
P3h2tm1Hpb/P3h2tm1Hpb involves: 129 * C57BL/6J |
abnormal thrombosis | J:206377 |
embryonic lethality during organogenesis, complete penetrance | J:206377 | |
embryonic lethality, incomplete penetrance | J:206377 |
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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last database update 12/10/2024 MGI 6.24 |
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