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Ectodermal Dysplasia v0.83 TUFT1 Zornitza Stark Publications for gene: TUFT1 were set to https://doi.org/10.1093/bjd/ljac026
Ectodermal Dysplasia v0.82 TUFT1 Zornitza Stark edited their review of gene: TUFT1: Changed publications: 36689522
Ectodermal Dysplasia v0.82 TUFT1 Zornitza Stark Phenotypes for gene: TUFT1 were changed from Ectodermal dysplasia, MONDO:0019287, TUFT1-related to Woolly hair-skin fragility syndrome, MIM# 620415
Ectodermal Dysplasia v0.81 TUFT1 Zornitza Stark edited their review of gene: TUFT1: Changed phenotypes: Woolly hair-skin fragility syndrome, MIM# 620415
Ectodermal Dysplasia v0.77 TUFT1 Zornitza Stark Marked gene: TUFT1 as ready
Ectodermal Dysplasia v0.77 TUFT1 Zornitza Stark Gene: tuft1 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.77 TUFT1 Zornitza Stark Classified gene: TUFT1 as Amber List (moderate evidence)
Ectodermal Dysplasia v0.77 TUFT1 Zornitza Stark Gene: tuft1 has been classified as Amber List (Moderate Evidence).
Ectodermal Dysplasia v0.76 TUFT1 Zornitza Stark gene: TUFT1 was added
gene: TUFT1 was added to Ectodermal Dysplasia. Sources: Expert Review
Mode of inheritance for gene: TUFT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TUFT1 were set to https://doi.org/10.1093/bjd/ljac026
Phenotypes for gene: TUFT1 were set to Ectodermal dysplasia, MONDO:0019287, TUFT1-related
Review for gene: TUFT1 was set to AMBER
Added comment: 9 individuals from three families reported with woolly hair and skin fragility. One of the variants, c.60+1G>A was present in two of the families, founder effect demonstrated by haplotype analysis. Another loss of function variant present in the third family. Some functional data but mostly expression studies.
Sources: Expert Review