Gene: A2ML1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1 		0.600 Biomarker disease GENOMICS_ENGLAND Expansion of the RASopathies. 27942422 2016
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1 		0.600 Biomarker disease GENOMICS_ENGLAND External ear anomalies and hearing impairment in Noonan Syndrome. 25862627 2015
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1 		0.600 GermlineCausalMutation disease ORPHANET Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. 24939586 2015
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1 		0.600 Biomarker disease CLINGEN Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. 24939586 2015
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1 		0.600 Biomarker disease CLINGEN External ear anomalies and hearing impairment in Noonan Syndrome. 25862627 2015