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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Spry2
sprouty RTK signaling antagonist 2
MGI:1345138
31 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Ednrbs-36Pub/Ednrb+
Spry2tm1.1Mrt/Spry2+
involves: 101/Rl * 129P2/OlaHsd * C3H/Rl * C57BL/6J
abnormal palatal rugae morphology J:125229
cleft secondary palate J:125229
Ednrbs-36Pub/Ednrbs-36Pub
Tg(Spry2)2Tpo/0
B6.Cg-Ednrbs-36Pub Tg(Spry2)2Tpo
abnormal palate bone morphology J:125229
cleft secondary palate J:125229
normal craniofacial phenotype J:125229
maxillary shelf hypoplasia J:125229
Ednrbs-36Pub/Ednrbs-36Pub
Tg(Spry2)69Tpo/0
B6.Cg-Ednrbs-36Pub Tg(Spry2)69Tpo
abnormal palate bone morphology J:125229
cleft secondary palate J:125229
normal craniofacial phenotype J:125229
maxillary shelf hypoplasia J:125229
Fgfr1tm1.1Jpa/Fgfr1+
Spry2tm1.1Mrt/Spry2tm1.1Mrt
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
supernumerary teeth J:119280
Fgfr2tm1.1Dor/Fgfr2+
Spry2tm1.1Mrt/Spry2tm1.1Mrt
involves: 129P2/OlaHsd * 129X1/SvJ
normal craniofacial phenotype J:119280
Krastm4.1Tyj/Kras+
Spry2tm1Mrt/Spry2tm1Mrt
involves: 129P2/OlaHsd
increased lung tumor incidence J:119477
Krastm4Tyj/Kras+
Spry2tm1.1Mrt/Spry2tm1.1Mrt
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N
impaired branching involved in bronchus morphogenesis J:119477
Ptentm2.1Ppp/Pten+
Spry1tm1Jdli/Spry1tm1.1Jdli
Spry2tm1Mrt/Spry2tm1.1Mrt
Tg(Osr1-cre)4Mrt/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N
increased prostate gland tumor incidence J:192348
increased prostate intraepithelial neoplasia incidence J:192348
Ptentm2.1Ppp/Ptentm2.1Ppp
Tg(CAG-Bgeo,-Spry2,-ALPP)1Mrt/0
Tg(Osr1-cre)4Mrt/0
involves: 129P2/OlaHsd * 129S1/Sv * FVB/N
increased prostate intraepithelial neoplasia incidence J:192348
Spry1tm1Jdli/Spry1tm1.1Jdli
Spry2tm1Mrt/Spry2tm1.1Mrt
Tg(Osr1-cre)4Mrt/0
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N
increased prostate intraepithelial neoplasia incidence J:192348
prostate gland epithelial hyperplasia J:192348
Spry2tm1.1Mrt/Spry2+
Spry4tm1.2Mrt/Spry4tm1.2Mrt
involves: 129P2/OlaHsd
abnormal autopod morphology J:315670
abnormal chondrocyte morphology J:315670
abnormal primary cilium morphology J:315670
abnormal skeleton morphology J:315670
increased enchondroma incidence J:315670
increased osteochondroma incidence J:315670
short tibia J:315670
Spry2tm1.1Mrt/Spry2tm1.1Mrt
Spry4tm1.2Mrt/Spry4+
involves: 129P2/OlaHsd
abnormal autopod morphology J:315670
abnormal skeleton morphology J:315670
increased enchondroma incidence J:315670
increased osteochondroma incidence J:315670
Spry2tm1Ayos/Spry2+
Spry4tm1Ayos/Spry4tm1Ayos
involves: 129 * C57BL/6J
decreased body weight J:116506
perinatal lethality, incomplete penetrance J:116506
postnatal lethality, incomplete penetrance J:116506
Spry2tm1Ayos/Spry2tm1Ayos
Spry4tm1Ayos/Spry4+
involves: 129 * C57BL/6J
prenatal lethality, complete penetrance J:116506
Spry2tm1Ayos/Spry2tm1Ayos
Spry4tm1Ayos/Spry4tm1Ayos
involves: 129 * C57BL/6J
abnormal brain development J:116506
abnormal craniofacial morphology J:116506
abnormal forebrain development J:116506
abnormal limb morphology J:116506
abnormal lung development J:116506
abnormal respiratory conducting tube morphology J:116506
alobar holoprosencephaly J:116506
cyclopia J:116506
embryonic lethality during organogenesis, incomplete penetrance J:116506
prenatal lethality, complete penetrance J:116506

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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
11/12/2024
MGI 6.24
The Jackson Laboratory