Gene: SAMD9L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 219285
Gene Symbol: SAMD9L
SAMD9L 		0.020 GeneticVariation group BEFREE Germline SAMD9 and SAMD9L mutations cause a spectrum of multisystem disorders that carry a markedly increased risk of developing myeloid malignancies with somatic monosomy 7. 30046003 2018
Entrez Id: 219285
Gene Symbol: SAMD9L
SAMD9L 		0.020 Biomarker group BEFREE Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7. 24029230 2013