Gene: RMRP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 CausalMutation disease CLINVAR Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP. 12107819 2002
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 CausalMutation disease CLINVAR Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia. 11207361 2001
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 GeneticVariation disease CLINVAR Astrobiology. Putting a lid on life on Europa. 11701897 2001
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 GeneticVariation disease CLINVAR Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia. 11207361 2001
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 CausalMutation disease CLINVAR Ribonuclease P: a ribonucleoprotein enzyme. 11006544 2000
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 CausalMutation disease CLINVAR Identification of adenosine functional groups involved in substrate binding by the ribonuclease P ribozyme. 10026268 1999
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 CausalMutation disease CLINVAR High-resolution genetic mapping of the cartilage-hair hypoplasia (CHH) gene in Amish and Finnish families. 8034306 1994
Entrez Id: 6023
Gene Symbol: RMRP
RMRP 		0.450 Biomarker disease CTD_human