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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ptprs
protein tyrosine phosphatase receptor type S
MGI:97815
59 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ptprdtm1Yiw/Ptprd+
Ptprstm1Mtr/Ptprstm1Mtr
B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr 		abnormal phrenic nerve morphology J:109122
decreased motor neuron number J:109122
Ptprdtm1Yiw/Ptprdtm1Yiw
Ptprstm1Mtr/Ptprs+
B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr 		abnormal phrenic nerve morphology J:109122
Ptprdtm1Yiw/Ptprdtm1Yiw
Ptprstm1Mtr/Ptprstm1Mtr
B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr 		abnormal brown adipose tissue morphology J:109122
abnormal motor neuron morphology J:109122
abnormal phrenic nerve morphology J:109122
abnormal pulmonary alveolus morphology J:109122
axial skeleton hypoplasia J:109122
carpoptosis J:109122
centrally nucleated skeletal muscle fibers J:109122
decreased motor neuron number J:109122
hypaxial muscle hypoplasia J:109122
increased subcutaneous adipose tissue amount J:109122
kyphosis J:109122
neonatal lethality, complete penetrance J:109122
thin dermal layer J:109122
thin diaphragm muscle J:109122
translucent skin J:109122
underdeveloped hair follicles J:109122
Ptprftm1Wjh/Ptprftm1Wjh
Ptprstm1Mtr/Ptprstm1Mtr
B6.Cg-Ptprftm1Wjh Ptprstm1Mtr 		abnormal basisphenoid bone morphology J:199299
abnormal first pharyngeal arch morphology J:199299
abnormal frontal bone morphology J:199299
abnormal interparietal bone morphology J:199299
abnormal mandible morphology J:199299
abnormal mandibular symphysis morphology J:199299
abnormal Meckel's cartilage morphology J:199299
abnormal nasal capsule morphology J:199299
abnormal neurocranium morphology J:199299
abnormal palatal mesenchymal cell proliferation J:199299
abnormal palate bone morphology J:199299
abnormal parietal bone morphology J:199299
abnormal premaxilla morphology J:199299
abnormal retina neuronal layer morphology J:149756
abnormal tongue morphology J:199299
abnormal ureter development J:149756
abnormal ureter morphology J:149756
absent nasal capsule J:199299
absent palatine bone J:199299
absent pterygoid process J:199299
absent tongue J:199299
cleft secondary palate J:149756, J:199299
decreased tongue size J:199299
dilated ureter J:149756
disorganized retina inner nuclear layer J:149756
double ureter J:149756
duplex kidney J:149756
exencephaly J:149756
eyelids open at birth J:149756
glossoptosis J:199299
hydroureter J:149756
mandible hypoplasia J:199299
micrognathia J:149756, J:199299
oral atresia J:199299
palatal shelves fail to meet at midline J:149756
persistent hyaloid artery J:149756
premature death J:149756
short mandible J:199299
short premaxilla J:199299
normal skeleton phenotype J:199299
small mandible J:199299
ureterocele J:149756
Ptprstm1Mtr/Ptprstm1Mtr
Rtn4rtm1.1Pado/Rtn4rtm1.1Pado
Rtn4rl1tm1.1Rojg/Rtn4rl1tm1.1Rojg
involves: 129S/SvEvBrd * 129S4/SvJae 		enhanced central nervous system regeneration J:191258
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory