| Monarch Ortholog Phenotypes
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Human (7 sources):
Global developmental delay,
Hemiplegia,
Intracranial hemorrhage,
Porencephalic cyst,
Seizure,
Spasticity,
Ventriculomegaly
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Mouse (48 sources):
abnormal atrioventricular cushion morphology,
abnormal cervical rib,
abnormal cranial blood vasculature morphology,
abnormal ductus venosus valve morphology,
abnormal eye muscle morphology,
abnormal hepatic vein morphology,
abnormal intestine placement,
abnormal left lung morphology,
abnormal lens epithelium morphology,
abnormal oculomotor nerve morphology,
abnormal optic cup morphology,
abnormal optic stalk morphology,
abnormal outer ear morphology,
abnormal right lung morphology,
abnormal tail morphology,
abnormal thymus topology,
abnormal thyroid gland isthmus morphology,
abnormal trigeminal ganglion morphology,
abnormal ventral pancreas morphology,
abnormal vertebral artery topology,
absent costovertebral joint,
absent ductus venosus valve,
absent thyroid gland isthmus,
additional anastomosis between intracranial vertebral arteries,
aphakia,
blood in lymph vessels,
corneal-lenticular stalk,
decreased circulating fructosamine level,
decreased circulating iron level,
decreased erythrocyte cell number,
decreased hematocrit,
decreased hemoglobin content,
embryo cyst,
embryo tumor,
fusion of vertebral arches,
heterochrony,
increased trigeminal neuroma incidence,
lethality throughout fetal growth and development, complete penetrance,
postnatal lethality, complete penetrance,
prenatal lethality, incomplete penetrance,
preweaning lethality, complete penetrance,
retroesophageal right subclavian artery,
retrolental blood,
small thymus,
small thyroid gland,
subcutaneous edema,
thoracoschisis,
vacuolated lens
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View all ortholog results at Monarch
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These phenotypes are associated with this gene with a has phenotype relation via Monarch.