PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35181734-2	2022	One such gene, tryptophan-aspartate repeat domain 72 (WDR72), has been found to cause a tooth enamel defect when deleted or mutated, resulting in a condition called amelogenesis imperfecta.	Aspartic Acid	26-35	WD repeat domain 72	Homo sapiens	54-59	
30028003-0	2018	Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations.	Aspartic Acid	51-60	WD repeat domain 72	Homo sapiens	79-84	
30028003-4	2018	Here, we report compound heterozygous pathogenic variations in tryptophan-aspartate repeat domain 72 (WDR72) (c.1777A>G [p.R593G] and c.2522T>A [p.L841Q]) in three affected siblings of a family with dRTA.	Aspartic Acid	74-83	WD repeat domain 72	Homo sapiens	102-107