Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 392636
Gene Symbol: AGMO
AGMO
0.310 GeneticVariation disease BEFREE A homozygous frameshift variant [p.(Glu324LysfsTer12)] in AGMO has recently been reported in two male siblings with syndromic microcephaly. 31555905 2019
Entrez Id: 392636
Gene Symbol: AGMO
AGMO
0.310 Biomarker disease GENOMICS_ENGLAND Biallelic variants in AGMO with diminished enzyme activity are associated with a neurodevelopmental disorder. 31555905 2019
Entrez Id: 392636
Gene Symbol: AGMO
AGMO
0.310 Biomarker disease GENOMICS_ENGLAND The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family. 27000257 2016