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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
F2rl1
F2R like trypsin receptor 1
MGI:101910
24 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
F2rtm1.1Cgh/F2rtm1.1Cgh
F2rl1tm2Cgh/F2rl1tm2Cgh
Tg(Tek-F2r)1Cgh/0
involves: 129S4/SvJae * C57BL/6
normal cardiovascular system phenotype J:157446
exencephaly J:157446
normal mortality/aging J:157446
F2rtm1Ajc/F2rtm1Ajc
F2rl1tm1Cgh/F2rl1tm1Cgh
involves: 129S4/SvJae
abnormal neural tube morphology J:188121
curly tail J:188121
spina bifida J:188121
F2rtm1Ajc/F2rtm1Ajc
F2rl1tm1Cgh/F2rl1tm1Cgh
involves: 129S4/SvJae * C57BL/6
decreased survivor rate J:132733
embryonic lethality, incomplete penetrance J:132733
increased susceptibility to endotoxin shock J:132733
increased susceptibility to induced morbidity/mortality J:132733
F2rtm1Ajc/F2rtm1Ajc
F2rl1tm1Cgh/F2rl1tm1Cgh
F2rl3tm1Cgh/F2rl3tm1Cgh
involves: 129S4/SvJae * C57BL/6
embryonic lethality J:132733
F2rtm2Cgh/F2r+
F2rl1tm2Cgh/F2rl1+
involves: 129S4/SvJae * C57BL/6
incomplete rostral neuropore closure J:157446
F2rl1tm1Bpd/F2rl1tm1Bpd
F3tm1.1Dwr/F3tm1.1Dwr
B6.129-F3tm1.1Dwr F2rl1tm1Bpd
normal cardiovascular system phenotype J:135087
F2rl1tm1Bpd/F2rl1tm1Bpd
Tg(MMTV-PyVT)634Mul/0
B6.Cg-F2rl1tm1Bpd Tg(MMTV-PyVT)634Mul
abnormal tumor vascularization J:138924
decreased mammary gland tumor incidence J:138924
increased adenoma incidence J:138924
increased mammary adenocarcinoma incidence J:138924
F2rl1tm1Cgh/F2rl1tm1Cgh
Spink5tm1Hov/Spink5tm1Hov
involves: 129P2/OlaHsd * 129S4/SvJae
abnormal epidermis stratum corneum morphology J:180855
abnormal skin morphology J:180855
abnormal vibrissa morphology J:180855
acanthosis J:180855
dehydration J:180855
neonatal lethality, complete penetrance J:180855
F2rl1tm1Cgh/F2rl1tm1Cgh
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
involves: 129P2/OlaHsd * 129S4/SvJae
embryonic lethality, complete penetrance J:188121
F2rl1tm1Cgh/F2rl1tm1Cgh
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
St14tm1Bug/St14+
involves: 129P2/OlaHsd * 129S4/SvJae
exencephaly J:188121
F2rl1tm1Cgh/F2rl1tm1Cgh
Tg(KRT14-Prss8)2Hum/?
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal integument phenotype J:189278

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory