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Repeat Disorders v0.123 HFGS_tract1 Zornitza Stark Tag paediatric-onset tag was added to STR: HFGS_tract1.
Repeat Disorders v0.26 HFGS_tract1 Bryony Thompson Marked STR: HFGS_tract1 as ready
Repeat Disorders v0.26 HFGS_tract1 Bryony Thompson Str: hfgs_tract1 has been classified as Green List (High Evidence).
Repeat Disorders v0.26 HFGS_tract1 Bryony Thompson Classified STR: HFGS_tract1 as Green List (high evidence)
Repeat Disorders v0.26 HFGS_tract1 Bryony Thompson Str: hfgs_tract1 has been classified as Green List (High Evidence).
Repeat Disorders v0.25 HFGS_tract1 Bryony Thompson STR: HFGS_tract1 was added
STR: HFGS_tract1 was added to Repeat Disorders. Sources: Expert list
Mode of inheritance for STR: HFGS_tract1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for STR: HFGS_tract1 were set to 10839976; 12073020; 33811808
Phenotypes for STR: HFGS_tract1 were set to Hand-foot-uterus syndrome MIM#140000
Review for STR: HFGS_tract1 was set to GREEN
STR: HFGS_tract1 was marked as clinically relevant
Added comment: NM_000522.5(HOXA13):c.126_128[X]
Expected mechanism of disease is a polyAlanine tract associated with dominant-negative effect or leading to a loss of function of the protein
PolyAla tract 1 of the 3 N-terminal polyAla tracts
Normal repeat number: 14-16
Pathogenic repeat number: 22
Sources: Expert list