Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 GeneticVariation disease UNIPROT ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. 22645276 2012
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 GeneticVariation disease UNIPROT Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects. 22068589 2012
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 Biomarker disease GENOMICS_ENGLAND Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects. 22068589 2012
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 GeneticVariation disease UNIPROT Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. 21441919 2011
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 Biomarker disease GENOMICS_ENGLAND Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. 11889557 2002
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 220202
Gene Symbol: ATOH7
ATOH7 		0.600 CausalMutation disease CLINVAR
Entrez Id: 23554
Gene Symbol: TSPAN12
TSPAN12 		0.100 CausalMutation disease CLINVAR