About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Procr
protein C receptor, endothelial
MGI:104596
32 phenotypes from 7 alleles in 11 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Meox2tm1(cre)Sor/Meox2+
Procrtm1Cte/Procrtm2Cte
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * Black Swiss * C57BL/6 		prenatal lethality, complete penetrance J:119529
Meox2tm1(cre)Sor/Meox2+
Procrtm2Cte/Procrtm2Cte
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * Black Swiss * C57BL/6 		abnormal hematopoietic system morphology/development J:119529
decreased circulating fibrinogen level J:119529
increased circulating C-reactive protein level J:119529
thrombocytopenia J:119529
Procrtm1.1(cre/ERT2)Yaz/Procrtm1.1(cre/ERT2)Yaz
involves: 129P2/OlaHsd * C57BL/6 		embryonic lethality during organogenesis, complete penetrance J:217483
Procrtm1.1Pcl/Procr+
involves: 129S2/SvPas * C57BL/6 		abnormal circulating protein level J:225914
Procrtm1.1Pcl/Procrtm1.1Pcl
involves: 129S2/SvPas * C57BL/6 		abnormal circulating protein level J:225914
bone marrow failure J:225914
decreased bone marrow cell number J:225914
enlarged spleen J:225914
extramedullary hematopoiesis J:225914
normal hematopoietic system phenotype J:225914
increased circulating interleukin-6 level J:225914
increased spleen red pulp amount J:225914
increased spleen weight J:225914
increased splenocyte number J:225914
increased susceptibility to endotoxin shock J:225914
increased susceptibility to induced thrombosis J:225914
normal mortality/aging J:225914
thrombocytopenia J:225914
Procrtm1Cte/Procr+
B6.129S7-Procrtm1Cte 		abnormal blood coagulation J:144388
thrombocytopenia J:144388
Procrtm1Cte/Procrtm1Cte
either: 129S/SvEv-Procrtm1Cte or (involves: 129S7/SvEvBrd * Black Swiss) 		abnormal blood coagulation J:80043
abnormal extraembryonic tissue morphology J:80043
abnormal placental thrombosis J:80043
decreased embryo size J:80043
embryonic growth retardation J:80043
embryonic lethality during organogenesis, complete penetrance J:80043
incomplete embryo turning J:80043
Procrtm1Cte/Procrtm1Cte
involves: 129S7/SvEvBrd 		prenatal lethality, incomplete penetrance J:119529
Procrtm1Cte/Procrtm1Cte
Tg(Tek-Procr)1Cte/0
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N 		embryonic lethality during organogenesis, complete penetrance J:119529
Procrtm1Fjc/Procrtm1Fjc
involves: 129X1/SvJ 		no abnormal phenotype detected J:80955
Procrtm2Cte/Procrtm3Cte
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 		normal mortality/aging J:144388
Procrtm3Cte/Procrtm3Cte
involves: 129S7/SvEvBrd * C57BL/6 		prenatal lethality, complete penetrance J:144388
Tg(Tek-Procr)1Cte/0
B6.FVB-Tg(Tek-Procr)1Cte 		abnormal acute phase protein level J:119637
abnormal blood coagulation J:119637
abnormal enzyme/coenzyme level J:119637
abnormal immune system physiology J:119637
abnormal inflammatory response J:119637
abnormal platelet physiology J:119637
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory