Gene: TRMT10A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 93587
Gene Symbol: TRMT10A
TRMT10A 		0.310 Biomarker disease GENOMICS_ENGLAND Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities. 26535115 2015
Entrez Id: 93587
Gene Symbol: TRMT10A
TRMT10A 		0.310 GeneticVariation disease BEFREE tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. 24204302 2013