Gene: LBR ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 Biomarker disease GENOMICS_ENGLAND Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR. 23824842 2013
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 GeneticVariation disease UNIPROT Methods In this context, a search was undertaken for mutations in LMNA, encoding Lamins A/C, and ZMPSTE24, LBR, LMNB1, LMNB2, MAN1, SYNE1a and LAP2, encoding Lamins A/C molecular partners, in a Caucasian woman affected with Reynolds syndrome, a particular nosologic entity specifically associating limited cutaneous SSc and primary biliary cirrhosis. 20522425 2010
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 GeneticVariation disease BEFREE LBR mutations might thus be associated with Reynolds syndrome. 20522425 2010
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 GeneticVariation disease ORPHANET Methods In this context, a search was undertaken for mutations in LMNA, encoding Lamins A/C, and ZMPSTE24, LBR, LMNB1, LMNB2, MAN1, SYNE1a and LAP2, encoding Lamins A/C molecular partners, in a Caucasian woman affected with Reynolds syndrome, a particular nosologic entity specifically associating limited cutaneous SSc and primary biliary cirrhosis. 20522425 2010
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 GeneticVariation disease CLINVAR
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 Biomarker disease CTD_human
Entrez Id: 3930
Gene Symbol: LBR
LBR 		0.710 CausalMutation disease CLINVAR