stag2 Phenotypes

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Phenotypes

Gene Literature (9)

Nucleotides (402)

Interactants (110)

XB-GENEPAGE-998551

Gene Symbol: stag2 Gene Name: STAG2 cohesin complex component

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (42 sources): Abnormal cardiac septum morphology, Abnormal facial shape, Attention deficit hyperactivity disorder, Bulbous nose, Cleft lip, Cleft palate, Clinodactyly of the 5th finger, Coarctation of aorta, Congenital diaphragmatic hernia, Curly eyelashes, Delayed ability to walk, Delayed speech and language development, Depressed nasal bridge, Failure to thrive, Frontal bossing, Full cheeks, Generalized hypotonia, Global developmental delay, High anterior hairline, Hypoplastic left heart, Long philtrum, Low anterior hairline, Low-set ears, Microcephaly, Micrognathia, Microtia, Pes planus, Polydactyly, Preauricular pit, Preauricular skin tag, Prominent nose, Proptosis, Scoliosis, Sensorineural hearing impairment, Short philtrum, Short stature, Sloping forehead, Smooth philtrum, Thin upper lip vermilion, Triangular face, Unsteady gait, Wide nasal bridge [+]
Mouse (15 sources): abnormal cardiac outflow tract development, abnormal enterocyte proliferation, abnormal heart development, abnormal hematopoietic stem cell physiology, abnormal mitosis, cellular necrosis, decreased cell proliferation, decreased embryo size, decreased fibroblast proliferation, decreased heart right ventricle size, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, hematopoietic system phenotype, increased fibroblast apoptosis, premature death [+]
View all ortholog results at Monarch