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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Bmpr2
bone morphogenetic protein receptor, type II (serine/threonine kinase)
MGI:1095407
49 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Acvr2atm1Hsch/Acvr2a+
Bmpr2tm1.1Enl/Bmpr2tm1.1Enl
Tg(KRT14-cre)1Ipc/0
involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * SJL
abnormal auchene hair morphology J:189569
abnormal awl hair morphology J:189569
abnormal coat/ hair morphology J:189569
abnormal hair cycle J:189569
abnormal hair cycle catagen phase J:189569
abnormal hair follicle outer root sheath morphology J:189569
abnormal hair follicle regression J:189569
abnormal hair growth J:189569
abnormal hair medulla J:189569
abnormal hair medullary septa cells J:189569
abnormal hair shaft melanin granule distribution J:189569
abnormal hair shaft morphology J:189569
abnormal zigzag hair morphology J:189569
absent hair club J:189569
alopecia J:189569
early exit from anagen phase J:189569
early exit from telogen phase J:189569
increased curvature of awl hairs J:189569
increased curvature of guard hairs J:189569
increased hair follicle cell proliferation J:189569
long nails J:189569
premature hair regrowth J:189569
striated fur J:189569
thick epidermis J:189569
thin hair shaft J:189569
Acvr2atm1Hsch/Acvr2atm1Hsch
Bmpr2tm1.1Enl/Bmpr2tm1.1Enl
Tg(KRT14-cre)1Ipc/0
involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * SJL
abnormal hair follicle development J:189569
abnormal hair growth J:189569
abnormal vibrissa follicle morphology J:189569
absent hair follicle bulb J:189569
absent vibrissae J:189569
eyelids open at birth J:189569
perinatal lethality, complete penetrance J:189569
underdeveloped hair follicles J:189569
Acvr2atm1Hsch/Acvr2atm1Hsch
Bmpr2tm1.1Enl/Bmpr2tm1.1Enl
Tg(Tyr-cre)1Lru/Y
involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2
abnormal coat/hair pigmentation J:189569
abnormal hair follicle melanin granule morphology J:189569
diluted coat color J:189569
reduced hair shaft melanin granule number J:189569
small melanosome J:189569
Acvr2atm1Hsch/Acvr2atm1Hsch
Bmpr2tm1.1Enl/Bmpr2tm1.1Enl
Tg(Tyr-cre)1Lru/0
involves: 129S1/Sv * 129S4/SvJae * C57BL/6 * DBA/2
mosaic coat color J:189569
Bmpr2tm1Kmi/Bmpr2+
Btg2tm1Spo/Btg2tm1Spo
involves: 129S4/SvJae * C57BL/6
vertebral transformation J:95124
Bmpr2tm1Kmi/Bmpr2+
Rnf165Gt(P9-3F)Sor/Rnf165+
Tg(Hlxb9-GFP)1Tmj/0
involves: 129S4/SvJae * C57BL/6 * CBA
abnormal motor neuron innervation pattern J:198828
decreased grip strength J:198828
prenatal lethality, incomplete penetrance J:198828
Bmpr2tm1Mmue/Bmpr2+
Smad1tm1Rjle/Smad1+
involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6
heart right ventricle hypertrophy J:224752
increased right ventricle systolic pressure J:224752
Tg(Tagln-rtTA)E1Jwst/0
Tg(tetO-BMPR2*T504)1Jwst/0
involves: FVB/N
abnormal heart ventricle morphology J:98898
abnormal vascular smooth muscle morphology J:98898
hypertension J:98898
increased heart right ventricle weight J:98898
increased hematocrit J:98898
increased right ventricle systolic pressure J:98898

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/16/2019
MGI 6.13
The Jackson Laboratory