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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		P3h1
prolyl 3-hydroxylase 1
MGI:1888921
30 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
P3h1tm1.1Brle/P3h1tm1.1Brle
involves: 129S7/SvEvBrd * C57BL/6 		abnormal bone collagen fibril morphology J:204353
abnormal trabecular bone morphology J:204353
decreased bone mineral density J:204353
decreased bone trabecula number J:204353
decreased trabecular bone mass J:204353
decreased trabecular bone thickness J:204353
decreased trabecular bone volume J:204353
P3h1tm1b(EUCOMM)Wtsi/P3h1tm1b(EUCOMM)Wtsi
C57BL/6N-P3h1tm1b(EUCOMM)Wtsi/Ucd 		abnormal limb position J:211773
abnormal skeletal muscle morphology J:211773
abnormal skin morphology J:211773
decreased body length J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased grip strength J:211773
decreased locomotor activity J:211773
increased total body fat amount J:211773
prolonged RR interval J:211773
thin skin J:211773
P3h1tm1Dgen/P3h1tm1Dgen
involves: C57BL/6 		abnormal dermal layer morphology J:163884
abnormal dermis reticular layer collagen network J:163884
abnormal femur morphology J:163884
abnormal long bone hypertrophic chondrocyte zone J:163884
abnormal tendon morphology J:163884
abnormal trabecular bone morphology J:163884
decreased body size J:163884
decreased bone mineral density J:163884
decreased length of long bones J:163884
decreased total body fat amount J:163884
delayed bone ossification J:163884
disproportionate dwarf J:163884
kyphoscoliosis J:163884
postnatal growth retardation J:163884
short femur J:163884
thin skin J:163884
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
12/10/2024
MGI 6.24 		The Jackson Laboratory