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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Spry2
sprouty RTK signaling antagonist 2
MGI:1345138
64 phenotypes from 4 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Mesp1tm2(cre)Ysa/Mesp1+
Tg(CAG-Bgeo,-Spry2,-ALPP)1Mrt/0
involves: C57BL/6NCrlj * CBA/JNCrlj
abnormal cardiac epithelial to mesenchymal transition J:143444
abnormal cardiac outflow tract development J:143444
abnormal heart development J:143444
abnormal heart morphology J:143444
atrioventricular septal defect J:143444
bicuspid aortic valve J:143444
double outlet right ventricle J:143444
persistent truncus arteriosus J:143444
ventricular septal defect J:143444
Pax3tm1(cre)Joe/Pax3+
Tg(CAG-Bgeo,-Spry2,-ALPP)1Mrt/0
Not Specified
normal cardiovascular system phenotype J:143444
short mandible J:143444
short snout J:143444
Spry2tm1.1Mrt/Spry2tm1.1Mrt
involves: 129/Sv * 129P2/OlaHsd * Black Swiss * C57BL/6 * FVB/N
abnormal auditory brainstem response waveform shape J:98303
abnormal Claudius cell morphology J:98303
abnormal digestive system physiology J:98303
abnormal organ of Corti morphology J:98303
abnormal organ of Corti supporting cell morphology J:98303
abnormal pillar cell morphology J:98303
decreased body size J:98303
increased cochlear outer hair cell number J:98303
increased Deiters cell number J:98303
increased or absent threshold for auditory brainstem response J:98303
postnatal lethality, incomplete penetrance J:98303
Spry2tm1.1Mrt/Spry2tm1.1Mrt
involves: 129P2/OlaHsd
abnormal chondrocyte morphology J:315670
abnormal craniofacial bone morphology J:315670
abnormal diastema morphology J:119280
abnormal mandible morphology J:315670
abnormal mandibular condyloid process morphology J:315670
abnormal mandibular coronoid process morphology J:315670
abnormal maxillary shelf morphology J:315670
abnormal molar cusp morphology J:119280
abnormal neurocranium morphology J:315670
abnormal primary cilium morphology J:315670
abnormal temporal bone morphology J:315670
abnormal tooth development J:119280
abnormal tooth morphology J:315670
abnormal vertebral arch morphology J:315670
abnormal vertebral spinous process morphology J:315670
abnormal vertebral transverse process morphology J:315670
cleft palate J:315670
complete cleft palate J:315670
decreased bone mineral density J:315670
decreased length of long bones J:315670
decreased trabecular bone mass J:315670
enlarged frontal bone J:315670
enlarged interparietal bone J:315670
increased cranium height J:315670
increased long bone epiphyseal plate size J:315670
malocclusion J:315670
short nasal bone J:315670
short snout J:315670
small neurocranium J:315670
small supraoccipital bone J:315670
small vertebral body J:315670
spinal stenosis J:315670
supernumerary teeth J:119280, J:315670
wide intermaxillary suture J:315670
Spry2tm1Ayos/Spry2tm1Ayos
B6.Cg-Spry2tm1Ayos
abnormal digestive system physiology J:99827
abnormal enteric ganglia morphology J:99827
abnormal enteric nervous system morphology J:99827
abnormal enteric neuron morphology J:99827
abnormal intestine morphology J:99827
decreased body size J:99827
dilated esophagus J:99827
intestinal obstruction J:99827
premature death J:99827
Spry2tm1Mrt/Spry2tm1Mrt
involves: 129P2/OlaHsd
increased lung tumor incidence J:119477

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
04/23/2024
MGI 6.23
The Jackson Laboratory