Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 Biomarker disease BEFREE SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptase. 30445423 2019
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 GeneticVariation disease BEFREE We found only one other report of an optic nerve coloboma associated with SPINT2 mutations and this occurred in a patient with congenital tufting enteropathy. 29575628 2018
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 GeneticVariation disease BEFREE Our data indicate that the loss of HAI-2 in Prss8R44Q/R44Q mice leads to development of progressive intestinal failure that at both histological and molecular level bears a striking resemblance to human congenital tufting enteropathy, and may provide important clues for understanding and treating this debilitating human disease. 29617460 2018
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 GeneticVariation disease BEFREE Recent cases of syndromic tufting enteropathy harboring the SPINT2 (19q13.2) mutation were described. 26684320 2016
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 Biomarker disease GENOMICS_ENGLAND Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form. 24142340 2014
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
0.350 Biomarker disease BEFREE Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form. 24142340 2014