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Proper Citation: RRID:MGI:5700966
Description: Allele Detail: Targeted This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Targeted This is a legacy resource.
Phenotype: absent maxilla, abnormal vitelline vein connection, abnormal inferior vena cava morphology, abnormal pelvic girdle bone morphology, double outlet right ventricle, abnormal forebrain morphology, abnormal thymus morphology, embryo cyst, abnormal posterior semicircular canal morphology, abnormal interatrial septum morphology, athymia, small salivary gland, rib fusion, abnormal brain commissure morphology, abnormal external auditory canal morphology, fusion of vertebral bodies, fusion of vertebral arches, abnormal middle ear ossicle morphology, absent brain internal capsule, abnormal brain internal capsule morphology, abnormal midbrain morphology, thin cerebral cortex, abnormal semicircular canal morphology, abnormal optic cup morphology, abnormal optic stalk morphology, abnormal sphenoid bone morphology, intraembryonal intestine elongation, abnormal eye muscle morphology, abnormal parasellar internal carotid artery branch morphology, oligodactyly, absent olfactory nerve, abnormal ductus venosus valve topology, increased rib number, abnormal hypoglossal nerve topology, absent hypoglossal nerve, abnormal spinal cord central canal morphology, epithelioid cysts, absent trochlear nerve, blood in lymph vessels, absent connection between subcutaneous lymph vessels and lymph sac, abnormal femur morphology, abnormal choroid plexus morphology, thoracoschisis, trigeminal neuroma, abnormal nasal cavity morphology, abnormal nasal septum morphology, small superior cervical ganglion, abnormal vertebral artery origin, small kidney, persistent trigeminal artery, abnormal Wolffian duct morphology, abnormal dorsal root ganglion topology, absent abducens nerve, umbilical vein stenosis, absent segment of posterior cerebral artery, abnormal pineal gland morphology, absent vomeronasal organ, intestinal/bowel diverticulum, absent salivary gland, abnormal olfactory bulb morphology, abnormal salivary gland morphology, abnormal vertebral body morphology, perimembraneous ventricular septal defect, abnormal outer ear morphology, preweaning lethality, complete penetrance, abnormal bile duct morphology, fetal growth retardation, abnormal infrahyoid muscle connection, tongue hypoplasia, muscular ventricular septal defect, basal brain tissue herniation, abnormal thymus topology, aorta coarctation, short Meckel's cartilage, absent external auditory canal, spleen hypoplasia, abnormal lens morphology, holoprosencephaly, subcutaneous edema, aphakia, absent olfactory bulb, persistent truncus arteriosis, abnormal thyroid gland morphology, anastomosis between middle cerebral arteries, absent tongue, abnormal neurohypophysis morphology, herniated liver, abnormal adenohypophysis morphology, abnormal olfactory nerve morphology, abnormal oral cavity morphology, absent portal vein segment, absent optic chiasm, abnormal pulmonary artery origin, absent eye muscles, absent neurohypophysis, heterochrony, abnormal vomeronasal organ morphology, fragmented Meckel's cartilage, abnormal duodenum topology, abnormal larynx morphology, absent stapedial artery, abnormal hindbrain morphology, absent pineal gland, abnormal facial nerve topology, absent posterior commissure, absent celiac artery
Affected Gene: Psph
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Source: MGI
Source Database: MGI, Mouse Genome Informatics MGI
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