About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
F2r
coagulation factor II thrombin receptor
MGI:101802
63 phenotypes from 4 alleles in 8 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
F2rtm1Ajc/F2rtm1Ajc
B6.129S4-F2rtm1Ajc
abnormal bone volume J:217458
abnormal cell physiology J:76348
abnormal circulating protein level J:217458
abnormal neuron apoptosis J:89774
abnormal sinus venosus morphology J:71309
abnormal urine protein level J:217458
abnormal vitelline vasculature morphology J:71309
absent vitelline blood vessels J:71309
decreased bone trabecular spacing J:217458
decreased compact bone thickness J:217458
decreased tumor necrosis factor (ligand) superfamily member 11 level J:217458
distended pericardium J:71309
embryonic growth retardation J:71309
embryonic lethality during organogenesis, incomplete penetrance J:71309
hemopericardium J:71309
hemorrhage J:71309
normal homeostasis/metabolism phenotype J:217458
increased body weight J:217458
increased bone mineral density J:217458
increased bone trabecula number J:217458
increased compact bone volume J:217458
increased trabecular bone volume J:217458
increased tumor necrosis factor receptor superfamily member 11b level J:217458
increased urine pH J:217458
increased urine sodium level J:217458
long femur J:217458
normal neoplasm J:92278
polyuria J:217458
normal skeleton phenotype J:217458
F2rtm1Ajc/F2rtm1Ajc
involves: 129S4/SvJae
curly tail J:188121
embryonic lethality during organogenesis, incomplete penetrance J:33380
F2rtm1Ajc/F2rtm1Ajc
involves: 129S4/SvJae * C57BL/6
abnormal gallbladder physiology J:123689
normal immune system phenotype J:132733
F2rtm1Ajc/F2rtm1Ajc
involves: 129S4/SvJae * C57BL/6J
abnormal cell physiology J:33380
abnormal placenta development J:33380
absent heartbeat J:33380
decreased embryo size J:33380
embryonic growth retardation J:33380
embryonic lethality during organogenesis, incomplete penetrance J:33380
normal hematopoietic system phenotype J:33380
F2rtm1Pago/F2rtm1Pago
B6.129P2-F2rtm1Pago
abnormal heart left ventricle morphology J:142990
abnormal response to cardiac infarction J:142990
normal cardiovascular system phenotype J:135087
normal immune system phenotype J:88245
F2rtm1Pago/F2rtm1Pago
involves: 129P2/OlaHsd
abnormal cytokine level J:133917
abnormal lymph node morphology J:133917
decreased susceptibility to endotoxin shock J:133917
decreased susceptibility to induced morbidity/mortality J:133917
enlarged mesenteric lymph nodes J:133917
F2rtm1Pago/F2rtm1Pago
involves: 129P2/OlaHsd * C57BL/6
abnormal blood pressure regulation J:38032
abnormal carotid artery morphology J:103347
abnormal fertility/fecundity J:38032
abnormal intestine physiology J:96182
abnormal systemic arterial blood pressure J:96312
abnormal systemic arterial blood pressure regulation J:38032
abnormal vascular wound healing J:103347
normal cardiovascular system phenotype J:38032, J:124465
decreased inflammatory response J:124648
decreased susceptibility to induced colitis J:94420
decreased vascular permeability J:124465
embryonic lethality during organogenesis, incomplete penetrance J:38032
F2rtm2Cgh/F2rtm2Cgh
involves: 129S4/SvJae * C57BL/6
abnormal cardiovascular system physiology J:157446
curly tail J:157446
decreased survivor rate J:157446
edema J:157446
exencephaly J:157446
lethality throughout fetal growth and development, incomplete penetrance J:157446
spina bifida J:157446
Tg(Myh6-F2r)18Nmk/0
involves: C57BL/6J
abnormal cardiovascular system physiology J:142990
dilated heart left ventricle J:142990
enlarged heart J:142990
increased heart weight J:142990

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
12/10/2024
MGI 6.24
The Jackson Laboratory