Gene: INHBB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3625
Gene Symbol: INHBB
INHBB 		0.020 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009
Entrez Id: 3625
Gene Symbol: INHBB
INHBB 		0.020 GeneticVariation disease BEFREE To investigate whether mutation of a gene in proximity to the chromosome 2 breakpoint underlies the SHFLD, we sought independent evidence of mutations in GLI2, INHBB and two other genes (RALB and FLJ14816) in 44 unrelated patients with SHFM, SHFLD or isolated long bone deficiency. 17569090 2007