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RIT1
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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GTP-binding protein Rit1 is a protein that in humans is encoded by the RIT1 gene.[5][6][7]
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Function
RIT belongs to the RAS (HRAS; MIM 190020) subfamily of small GTPases (Hynds et al., 2003).[supplied by OMIM][7]
Clinical significance
Mutations in RIT1 are associated to Noonan syndrome.[8]
Interactions
RIT1 has been shown to interact with KLHL12[9] and Merlin.[10]
References
Further reading
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