Activity

Filter

Cancel
Date Panel Item Activity
11 actions
Vitamin metabolism disorders v0.32 MTRR Bryony Thompson Marked gene: MTRR as ready
Vitamin metabolism disorders v0.32 MTRR Bryony Thompson Gene: mtrr has been classified as Green List (High Evidence).
Vitamin metabolism disorders v0.32 MTRR Bryony Thompson Classified gene: MTRR as Green List (high evidence)
Vitamin metabolism disorders v0.32 MTRR Bryony Thompson Gene: mtrr has been classified as Green List (High Evidence).
Vitamin metabolism disorders v0.31 MTR Bryony Thompson Marked gene: MTR as ready
Vitamin metabolism disorders v0.31 MTR Bryony Thompson Gene: mtr has been classified as Green List (High Evidence).
Vitamin metabolism disorders v0.31 MTR Bryony Thompson Classified gene: MTR as Green List (high evidence)
Vitamin metabolism disorders v0.31 MTR Bryony Thompson Gene: mtr has been classified as Green List (High Evidence).
Vitamin metabolism disorders v0.20 MTR Bryony Thompson Deleted their review
Vitamin metabolism disorders v0.12 MTR Bryony Thompson gene: MTR was added
gene: MTR was added to Inherited vitamin B12 or cobalamin deficiency. Sources: Literature
Mode of inheritance for gene: MTR was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MTR were set to 8968735; 27604308
Phenotypes for gene: MTR were set to Homocystinuria-megaloblastic anemia, cblG complementation type MIM#250940; Organic aciduria
Review for gene: MTR was set to GREEN
gene: MTR was marked as current diagnostic
Added comment: Sources: Literature
Vitamin metabolism disorders v0.10 MTRR Bryony Thompson gene: MTRR was added
gene: MTRR was added to Inherited vitamin B12 or cobalamin deficiency. Sources: Literature
Mode of inheritance for gene: MTRR was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MTRR were set to 27604308; 9501215
Phenotypes for gene: MTRR were set to Homocystinuria-megaloblastic anemia, cbl E type MIM#236270; Disorders of the metabolism of sulphur amino acids
Review for gene: MTRR was set to GREEN
gene: MTRR was marked as current diagnostic
Added comment: Sources: Literature