Searchable abstracts of presentations at key conferences in endocrinology

ea0049oc10.5 | Bone & Calcium Homeostasis | ECE2017

Gα11-Phe220Ser loss-of-function mutation causes familial hypocalciuric hypercalcemia type-2 (FHH2) by disrupting a hydrophobic cluster critical for G-protein signaling

Gorvin Caroline M. , Cranston Treena , Hannan Fadil M. , Valta Helena , Makitie Outi , Schalin-Jantti Camilla , Thakker Rajesh V.

Mutations of the calcium-sensing receptor (CaSR), G-protein alpha-11 subunit (Gα11), and adaptor protein-2 sigma subunit (AP2σ) resulting in a loss-of-function, cause familial hypocalciuric hypercalcemia types 1-3 (FHH1-3), respectively. We investigated a family with FHH (four affected and two unaffected members) for CaSR, Gα11 and AP2σ mutations, and identified a heterozygous Gα11 missense mutation, Phe220Ser, which is predicted to disrupt a cluster o...