NHP2, NHP2 ribonucleoprotein, 55651

N. diseases: 91; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 GeneticVariation disease BEFREE Since the number of patients with DC is small and the effect of genetic pathogenic variant may affect the phenotype, we wanted to present the clinical features and course of illness in a patient with NHP2 gene mutation (compound heterozygote for the NHP2 mutations c.376G>A/c.460T>A; amino acid substitutions: p.Val126Met and p.X154Arg) that occurred as a compound heterozygous state. 30472699 2019
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 Biomarker disease GENOMICS_ENGLAND Germline Genetic Predisposition to Hematologic Malignancy. 28297620 2017
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 Biomarker disease GENOMICS_ENGLAND The telomere syndromes. 22965356 2012
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 Biomarker disease GENOMICS_ENGLAND The telomere syndromes. 22965356 2012
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 GeneticVariation disease BEFREE We found that the most prevalent dyskerin mutation in DC (A353V) did not affect formation of the NAF1-dyskerin-NOP10-NHP2 tetramer that normally assembles with nascent H/ACA RNAs in vivo. 20008900 2010
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 Biomarker disease GENOMICS_ENGLAND We found that the most prevalent dyskerin mutation in DC (A353V) did not affect formation of the NAF1-dyskerin-NOP10-NHP2 tetramer that normally assembles with nascent H/ACA RNAs in vivo. 20008900 2010
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 GeneticVariation disease BEFREE Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita. 18523010 2008
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 Biomarker disease GENOMICS_ENGLAND Stable expression in yeast of the mature form of human telomerase RNA depends on its association with the box H/ACA small nucleolar RNP proteins Cbf5p, Nhp2p and Nop10p. 11160879 2001
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
0.430 CausalMutation disease CLINVAR