Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia. 9781036

1998

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT A novel missense mutation of the tissue-nonspecific alkaline phosphatase gene detected in a patient with hypophosphatasia. 9747027

1998

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT Hypophosphatasia: identification of five novel missense mutations (G507A, G705A, A748G, T1155C, G1320A) in the tissue-nonspecific alkaline phosphatase gene among Japanese patients. 9452105

1998

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia. 8954059

1996

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT Novel missense and frameshift mutations in the tissue-nonspecific alkaline phosphatase gene in a Japanese patient with hypophosphatasia. 7833929

1994

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites. 8406453

1993

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia. 1409720

1992

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 GeneticVariation UNIPROT A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia. 3174660

1988

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 Biomarker CTD_human

Entrez Id: 249
Gene Symbol: ALPL
ALPL
CUI: C0268413
Disease: Adult hypophosphatasia (disorder)
Adult hypophosphatasia (disorder)
0.950 Biomarker GENOMICS_ENGLAND