Gene: TINF2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26277
Gene Symbol: TINF2
TINF2 		0.310 GeneticVariation disease BEFREE We describe a child who presented with ataxia and pancytopenia and was found to have a heterozygous mutation, c.845G>A (Arg282His) in TINF2, a gene recently reported to be mutated in a subset of patients with autosomal dominant dyskeratosis congenita. 18979121 2008
Entrez Id: 26277
Gene Symbol: TINF2
TINF2 		0.310 Biomarker disease CTD_human