Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1
0.050 GeneticVariation disease BEFREE The proband's father had isolated preaxial polydactyly type II (PPD2). 25382487 2015
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1
0.050 Biomarker disease BEFREE This result suggests that Lmbr1 may underlie preaxial polydactyly in both mice and humans. 11606546 2001
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1
0.050 Biomarker disease BEFREE A recently proposed candidate gene for 7q36 linked preaxial polydactyly is LMBR1, encoding a novel transmembrane receptor which may be an upstream regulator of SHH. 11333865 2001
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1
0.050 GeneticVariation disease BEFREE The homeobox gene HLXB9, a putative receptor C7orf2, and two transcripts of unknown function, C7orf3 and C7orf4, map in the refined candidate region and have been subjected to mutation analysis in individuals with preaxial polydactyly. 10329000 1999
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1
0.050 GeneticVariation disease BEFREE We have characterized a 6-generation North American Caucasian kindred segregating one form of preaxial polydactyly type 2 (PPD-2). 8533803 1995