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Skeletal dysplasia v1.151 TERT Zornitza Stark Marked gene: TERT as ready
Skeletal dysplasia v1.151 TERT Zornitza Stark Gene: tert has been classified as Red List (Low Evidence).
Skeletal dysplasia v1.151 TERT Zornitza Stark Phenotypes for gene: TERT were changed from Dyskeratosis congenita, autosomal dominant 2 and autosomal recessive 4 613989 to Dyskeratosis congenita, MIM# 613989; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1, MIM# 614742
Skeletal dysplasia v1.150 TERT Zornitza Stark Publications for gene: TERT were set to
Skeletal dysplasia v1.149 TERT Zornitza Stark Classified gene: TERT as Red List (low evidence)
Skeletal dysplasia v1.149 TERT Zornitza Stark Gene: tert has been classified as Red List (Low Evidence).
Skeletal dysplasia v1.148 TERT Zornitza Stark edited their review of gene: TERT: Added comment: Not associated with skeletal dysplasia.; Changed rating: RED
Skeletal dysplasia v1.0 TERT Gene migrated from ENSG00000164362 to ENSG00000164362 (gene set migration)
Skeletal dysplasia v0.0 TERT Zornitza Stark gene: TERT was added
gene: TERT was added to Skeletal dysplasia. Sources: Expert list,NHS GMS,Expert Review Green,UKGTN,Illumina TruGenome Clinical Sequencing Services
Mode of inheritance for gene: TERT was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: TERT were set to Dyskeratosis congenita, autosomal dominant 2 and autosomal recessive 4 613989