Activity

Filter

Cancel
Date Panel Item Activity
12 actions
Pigmentary skin disorders v3.14 LMNA Achchuthan Shanmugasundram Tag Q1_24_promote_green was removed from gene: LMNA.
Tag Q1_24_NHS_review was removed from gene: LMNA.
Pigmentary skin disorders v3.14 LMNA Achchuthan Shanmugasundram reviewed gene: LMNA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Pigmentary skin disorders v3.13 LMNA Achchuthan Shanmugasundram Source Expert Review Green was added to LMNA.
Source NHS GMS was added to LMNA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Pigmentary skin disorders v3.10 LMNA Sarah Leigh Tag Q1_24_promote_green tag was added to gene: LMNA.
Tag Q1_24_NHS_review tag was added to gene: LMNA.
Pigmentary skin disorders v3.10 LMNA Sarah Leigh edited their review of gene: LMNA: Added comment: LMNA variants have been associated with various conditions, including Hutchinson-Gilford progeria (OMIM:176670) and Mandibuloacral dysplasia (OMIM:248370). Skin mottling has been reported in both of these conditions, and hyper and hypopigmentation is a feature of Mandibuloacral dysplasia (OMIM:248370). Numerous LMNA variants have been reported in these conditions.; Changed rating: GREEN
Pigmentary skin disorders v3.10 LMNA Sarah Leigh Classified gene: LMNA as Amber List (moderate evidence)
Pigmentary skin disorders v3.10 LMNA Sarah Leigh Gene: lmna has been classified as Amber List (Moderate Evidence).
Pigmentary skin disorders v3.9 LMNA Sarah Leigh Added comment: Comment on mode of inheritance: Hutchinson-Gilford progeria, OMIM:176670 is monoallelic, Mandibuloacral dysplasia, OMIM:248370 is biallelic
Pigmentary skin disorders v3.9 LMNA Sarah Leigh Mode of inheritance for gene: LMNA was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Pigmentary skin disorders v3.8 LMNA Sarah Leigh Phenotypes for gene: LMNA were changed from Hutchinson-Gilford progeria syndrome (HGPS) (MIM 176670); Mandibuloacral dysplasia with type A lipodystrophy (MADA) to Hutchinson-Gilford progeria, OMIM:176670; Hutchinson-Gilford progeria syndrome, MONDO:0008310; Mandibuloacral dysplasia, OMIM:248370; mandibuloacral dysplasia with type A lipodystrophy MONDO:0009557
Pigmentary skin disorders v3.7 LMNA Sarah Leigh Publications for gene: LMNA were set to PMID: 12714972; https://www.ncbi.nlm.nih.gov/books/NBK1121/#; 12075506; 17848409
Pigmentary skin disorders v3.6 LMNA Tom Cullup gene: LMNA was added
gene: LMNA was added to Pigmentary skin disorders. Sources: Expert list
Mode of inheritance for gene: LMNA was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: LMNA were set to PMID: 12714972; https://www.ncbi.nlm.nih.gov/books/NBK1121/#; 12075506; 17848409
Phenotypes for gene: LMNA were set to Hutchinson-Gilford progeria syndrome (HGPS) (MIM 176670); Mandibuloacral dysplasia with type A lipodystrophy (MADA)
Penetrance for gene: LMNA were set to Complete
Mode of pathogenicity for gene: LMNA was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Review for gene: LMNA was set to GREEN
Added comment: LMNA requested to be added to pigmentary disorders panel by Prof Kinsler, due to pigmentary lesions being an early sign of LMNA-progeria (AD).
Mottled pigmentation also a feature of MADA (AR).
Sources: Expert list