PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18448590-1	2008	A mutation in the human FXYD2 polypeptide (Na-K-ATPase gamma subunit) that changes a conserved transmembrane glycine to arginine is linked to dominant renal hypomagnesemia.	Glycine	109-116	FXYD domain containing ion transport regulator 2	Homo sapiens	24-29	
16828040-5	2006	Moreover, mutation of a conserved glycine residue into an arginine residue in FXYD2 has been linked to cases of human hypomagnesemia indicating that dysregulation of Na,K-ATPase by FXYD proteins may be implicated in pathophysiological states.	Glycine	34-41	FXYD domain containing ion transport regulator 2	Homo sapiens	78-83