Gene: NPAP1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 AlteredExpression disease BEFREE Because the Prader-Willi syndrome is known to be caused by the loss of function of paternally expressed genes in 15q11q13, a phenotypic contribution of NPAP1 cannot be excluded. 24482533 2014
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 Biomarker disease BEFREE The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. 22694955 2012
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 Biomarker disease BEFREE These results indicate that C15orf2 might have an important role in human biology and that a deficiency of C15orf2 might contribute to PWS. 20020165 2010
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 Biomarker disease BEFREE We conclude that PWRN1 and C15orf2 may play a role in PWS. 17337158 2007
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 Biomarker disease BEFREE Here we report the identification of a novel gene in the PWS critical region, which has been designated "chromosome 15 open reading frame 2" (C15orf2). 10783265 2000
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1 		0.350 Biomarker disease CTD_human