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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Psph
phosphoserine phosphatase
MGI:97788
128 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Psphtm1.1(KOMP)Vlcg/Psph+
C57BL/6N-Psphtm1.1(KOMP)Vlcg/Ucd
cardiovascular system phenotype J:211773
decreased circulating triglyceride level J:211773
increased heart rate variability J:211773
small adrenal glands J:211773
thrombocytopenia J:211773
Psphtm1.1(KOMP)Vlcg/Psphtm1.1(KOMP)Vlcg
C57BL/6N-Psphtm1.1(KOMP)Vlcg/Ucd
abnormal craniofacial morphology J:211773
abnormal embryo size J:211773
abnormal eye morphology J:211773
abnormal heart morphology J:211773
anophthalmia J:211773
edema J:211773
microphthalmia J:211773
pale placenta J:211773
pale yolk sac J:211773
pallor J:211773
preweaning lethality, complete penetrance J:211773
Psphtm1a(EUCOMM)Hmgu/Psphtm1a(EUCOMM)Hmgu
C57BL/6N-Psphtm1a(EUCOMM)Hmgu/Wtsi
abnormal adenohypophysis morphology J:239583
abnormal bile duct morphology J:239583
abnormal brain commissure morphology J:239583
abnormal brain internal capsule morphology J:239583
abnormal choroid plexus morphology J:239583
abnormal dorsal root ganglion topology J:239583
abnormal ductus venosus valve topology J:239583
abnormal duodenum topology J:239583
abnormal external auditory canal morphology J:239583
abnormal eye muscle morphology J:239583
abnormal facial nerve topology J:239583
abnormal femur morphology J:239583
abnormal forebrain morphology J:239583
abnormal hindbrain morphology J:239583
abnormal hypoglossal nerve topology J:239583
abnormal inferior vena cava morphology J:239583
abnormal infrahyoid muscle connection J:239583
abnormal interatrial septum morphology J:239583
abnormal larynx morphology J:239583
abnormal lens morphology J:239583
abnormal midbrain morphology J:239583
abnormal middle ear ossicle morphology J:239583
abnormal nasal cavity morphology J:239583
abnormal nasal septum morphology J:239583
abnormal neurohypophysis morphology J:239583
abnormal olfactory bulb morphology J:239583
abnormal olfactory nerve morphology J:239583
abnormal optic cup morphology J:239583
abnormal optic stalk morphology J:239583
abnormal oral cavity morphology J:239583
abnormal outer ear morphology J:239583
abnormal parasellar internal carotid artery branch morphology J:239583
abnormal pelvic girdle bone morphology J:239583
abnormal pineal gland morphology J:239583
abnormal placenta morphology J:261316
abnormal placental labyrinth vasculature morphology J:261316
abnormal posterior semicircular canal morphology J:239583
abnormal pulmonary artery origin J:239583
abnormal salivary gland morphology J:239583
abnormal semicircular canal morphology J:239583
abnormal sphenoid bone morphology J:239583
abnormal spinal cord central canal morphology J:239583
abnormal thymus morphology J:239583
abnormal thymus topology J:239583
abnormal thyroid gland morphology J:239583
abnormal trophoblast layer morphology J:261316
abnormal vertebral artery origin J:239583
abnormal vertebral body morphology J:239583
abnormal vitelline vein connection J:239583
abnormal vomeronasal organ morphology J:239583
abnormal Wolffian duct morphology J:239583
absent abducens nerve J:239583
absent brain internal capsule J:239583
absent celiac artery J:239583
absent connection between subcutaneous lymph vessels and lymph sac J:239583
absent external auditory canal J:239583
absent eye muscles J:239583
absent hypoglossal nerve J:239583
absent maxilla J:239583
absent neurohypophysis J:239583
absent olfactory bulb J:239583
absent olfactory nerve J:239583
absent optic chiasm J:239583
absent pineal gland J:239583
absent portal vein segment J:239583
absent posterior commissure J:239583
absent salivary gland J:239583
absent segment of posterior cerebral artery J:239583
absent stapedial artery J:239583
absent tongue J:239583
absent trochlear nerve J:239583
absent vomeronasal organ J:239583
anastomosis between middle cerebral arteries J:239583
aorta coarctation J:239583
aphakia J:239583
athymia J:239583
basal brain tissue herniation J:239583
blood in lymph vessels J:239583
double outlet right ventricle J:239583
embryo cyst J:239583
embryonic growth retardation J:261316
epithelioid cyst J:239583
fetal growth retardation J:239583
fragmented Meckel's cartilage J:239583
fusion of vertebral arches J:239583
fusion of vertebral bodies J:239583
herniated liver J:239583
heterochrony J:239583
holoprosencephaly J:239583
increased rib number J:239583
increased trigeminal neuroma incidence J:239583
intestinal/bowel diverticulum J:239583
intraembryonal intestine elongation J:239583
muscular ventricular septal defect J:239583
oligodactyly J:239583
perimembraneous ventricular septal defect J:239583
persistent trigeminal artery J:239583
persistent truncus arteriosus J:239583
placenta hemorrhage J:261316
placenta necrosis J:261316
preweaning lethality, complete penetrance J:211773, J:261316
rib fusion J:239583
short Meckel's cartilage J:239583
small kidney J:239583
small placenta J:261316
small salivary gland J:239583
small superior cervical ganglion J:239583
spleen hypoplasia J:239583
subcutaneous edema J:239583, J:261316
thin cerebral cortex J:239583
thoracoschisis J:239583
tongue hypoplasia J:239583
umbilical vein stenosis J:239583

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
12/10/2024
MGI 6.24
The Jackson Laboratory