SGO1 Chromosome 3

Shugoshin 1
2 variants 2 Health Risk

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What This Gene Does
The protein encoded by this gene is a member of the shugoshin family of proteins. This protein is thought to protect centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression of this gene leads to the premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest. Evidence suggests that this protein also protects a small subset of cohesin found along the length of the chromosome arms during mitotic prophase. An isoform lacking exon 6 has been shown to play a role in the cohesion of centrioles (PMID: 16582621 and PMID:18331714). Mutations in this gene have been associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by the co-occurrence of Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO) within the first four decades of life (PMID:25282101). Fibroblast cells from CAID patients exhibited both increased cell proliferation and higher rates of senescence. Pseudogenes of this gene have been found on chromosomes 1 and 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]
Associated Conditions (6)
Clear cell carcinoma of kidney
Lung cancer
Familial cancer of breast
Chronic atrial and intestinal dysrhythmia
Cardiovascular phenotype
SGO1-related disorder
Key Variants
All Variants (2)
RSID Category Clinical Significance Conditions
RS142110258 Health Risk Conflicting classifications of pathogenicity Clear cell carcinoma of kidney, Lung cancer, Familial cancer of breast
RS199815268 Health Risk Pathogenic Chronic atrial and intestinal dysrhythmia, Cardiovascular phenotype, SGO1-related disorder
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