TECTA, tectorin alpha, 7007

N. diseases: 24; N. variants: 28
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
0.020 GeneticVariation disease BEFREE To our knowledge, this is the first reported TECTA mutation leading to the DFNB21 form of hearing impairment among Maghrebian individuals suffering from congenital hearing impairment, which further illustrates the diversity of the genes involved in congenital deafness in the Maghreb. 27368438 2016
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
0.020 Biomarker disease BEFREE Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane. 24363064 2014