Gene: TTC7A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57217
Gene Symbol: TTC7A
TTC7A 		0.760 CausalMutation disease CLINVAR Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. 23830146 2013
Entrez Id: 57217
Gene Symbol: TTC7A
TTC7A 		0.760 GermlineCausalMutation disease ORPHANET Based on our genetic results, TTC7A is the likely causal gene for MIA. 23423984 2013
Entrez Id: 57217
Gene Symbol: TTC7A
TTC7A 		0.760 Biomarker disease CTD_human
Entrez Id: 57217
Gene Symbol: TTC7A
TTC7A 		0.760 Biomarker disease GENOMICS_ENGLAND