stag1 Phenotypes

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Phenotypes

XB-GENEPAGE-1006154

Gene Symbol: stag1 Gene Name: STAG1 cohesin complex component

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (15 sources): Cerebral atrophy, Cryptorchidism, Deeply set eye, Delayed speech and language development, Feeding difficulties, Gastroesophageal reflux, Generalized hypotonia, Global developmental delay, Intellectual disability, Microcephaly, Prominent nasal bridge, Seizure, Thin eyebrow, Wide mouth, Widely-spaced incisors [+]
Mouse (31 sources): abnormal bone mineralization, abnormal definitive hematopoiesis, abnormal kidney collecting duct morphology, abnormal kidney morphology, abnormal mammary gland morphology, abnormal mitosis, abnormal renal glomerulus morphology, abnormal telomere morphology, abnormal tooth development, aneuploidy, decreased brown adipose tissue amount, decreased cell proliferation, decreased fetal size, decreased fibroblast proliferation, decreased hair follicle number, decreased incidence of tumors by chemical induction, decreased tumor growth/size, delayed intramembranous bone ossification, embryonic lethality during organogenesis, incomplete penetrance, increased hepatocellular carcinoma incidence, increased histiocytic sarcoma incidence, increased lymphoma incidence, increased papilloma incidence, increased tumor incidence, lethality throughout fetal growth and development, complete penetrance, premature aging, premature death, preweaning lethality, complete penetrance, small kidney, small liver, urinary bladder obstruction [+]
View all ortholog results at Monarch