Gene: HOXA10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3206
Gene Symbol: HOXA10
HOXA10 		0.040 GeneticVariation disease BEFREE The results demonstrated that mutation in HOXA10 gene contributes to the pathogenesis of cryptorchidism, but may not be a common cause. 27108669 2017
Entrez Id: 3206
Gene Symbol: HOXA10
HOXA10 		0.040 GeneticVariation disease BEFREE Mutations in the human genes encoding insulin-like factor 3 (INSL3) and its Leu-rich repeat-containing G protein-coupled receptor 8 (LGR8), homeobox A10 (HOXA10), zinc finger 214 (ZNF214) and 215 (ZNF215) have occasionally been identified but do not seem to be a frequent cause of cryptorchidism. 20980787 2010
Entrez Id: 3206
Gene Symbol: HOXA10
HOXA10 		0.040 GeneticVariation disease BEFREE These data on HOXA10 analysis indicate that alterations of this gene may be more rare in males with cryptorchidism than previously suggested. 14960020 2004
Entrez Id: 3206
Gene Symbol: HOXA10
HOXA10 		0.040 GeneticVariation disease BEFREE Because to our knowledge this gene has never been examined for alterations in humans, we evaluated whether mutations of HOXA10 are associated with cryptorchidism in humans. 10037424 1999