Gene: INVS ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27130
Gene Symbol: INVS
INVS 		0.500 GermlineCausalMutation disease ORPHANET Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis. 22819833 2012
Entrez Id: 27130
Gene Symbol: INVS
INVS 		0.500 GermlineCausalMutation disease ORPHANET Retinitis pigmentosa and renal failure in a patient with mutations in INVS. 16522655 2006
Entrez Id: 27130
Gene Symbol: INVS
INVS 		0.500 Biomarker disease GENOMICS_ENGLAND Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. 12872123 2003