nsd1 Phenotypes

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Phenotypes

Gene Literature (7)

Nucleotides (180)

Interactants (159)

XB-GENEPAGE-989205

Gene Symbol: nsd1 Gene Name: nuclear receptor binding SET domain protein 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (73 sources): Abnormal cardiac septum morphology, Abnormal fingernail morphology, Abnormality of immune system physiology, Abnormality of the kidney, Abnormality of the ureter, Accelerated skeletal maturation, Advanced eruption of teeth, Anteverted nares, Aplasia/Hypoplasia of the corpus callosum, Atrial septal defect, Behavioral abnormality, Cavum septum pellucidum, Coarse facial features, Conductive hearing impairment, Congenital hip dislocation, Craniosynostosis, Cryptorchidism, Depressed nasal ridge, Dolichocephaly, Downslanted palpebral fissures, EEG abnormality, Enlarged cisterna magna, Expressive language delay, Feeding difficulties in infancy, Frontal bossing, Genu valgum, Genu varum, Global developmental delay, Glucose intolerance, High anterior hairline, High forehead, High palate, High, narrow palate, Hypermetropia, Hyperreflexia, Hypertelorism, Hypoglycemia, Hypospadias, Hypotonia, Intellectual disability, Large hands, Long foot, Macrocephaly, Macrotia, Mandibular prognathia, Micrognathia, Multiple renal cysts, Narrow palate, Neonatal hypotonia, Neoplasm, Neoplasm of the nervous system, Nephroblastoma, Nystagmus, Obesity, Otitis media, Partial agenesis of the corpus callosum, Patent ductus arteriosus, Pes planus, Pointed chin, Poor coordination, Precocious puberty, Prominent forehead, Renal duplication, Sacrococcygeal teratoma, Scoliosis, Seizure, Small nail, Strabismus, Tall stature, Ventricular septal defect, Ventriculomegaly, Vesicoureteral reflux, obsolete Joint laxity [+]
Mouse (10 sources): abnormal developmental patterning, abnormal egg cylinder morphology, abnormal extraembryonic tissue morphology, abnormal gastrulation movements, abnormal mesendoderm development, abnormal primitive streak morphology, abnormal rostral-caudal axis patterning, absent mesoderm, absent primitive node, embryonic lethality during organogenesis, complete penetrance
View all ortholog results at Monarch