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RIT1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

RIT1
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GTP-binding protein Rit1 is a protein that in humans is encoded by the RIT1 gene.[5][6][7]

Quick Facts Available structures, PDB ...
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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

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Further reading

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