Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6862
Gene Symbol: TBXT
TBXT
CUI: C3810343
Disease: SACRAL AGENESIS WITH VERTEBRAL ANOMALIES
SACRAL AGENESIS WITH VERTEBRAL ANOMALIES 		0.700 GeneticVariation UNIPROT Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal. 24253444

2014
Entrez Id: 6862
Gene Symbol: TBXT
TBXT
CUI: C3891448
Disease: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO 		0.400 GeneticVariation UNIPROT Autozygome and high throughput confirmation of disease genes candidacy. 30237576

2019
Entrez Id: 6862
Gene Symbol: TBXT
TBXT
CUI: C3891448
Disease: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO 		0.400 GeneticVariation UNIPROT The human T locus and spina bifida risk. 15449172

2004