Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies
Gene: HMGCREnsemblGeneIds (GRCh38): ENSG00000113161
EnsemblGeneIds (GRCh37): ENSG00000113161
OMIM: 142910, Gene2Phenotype
HMGCR is in 2 panels
3 reviews
Achchuthan Shanmugasundram (Genomics England Curator)
The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.Created: 5 Dec 2024, 5:12 p.m. | Last Modified: 5 Dec 2024, 5:12 p.m.
Panel Version: 4.40
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Sarah Leigh (Genomics England Curator)
HMGCR variants have been associated with Muscular dystrophy, limb-girdle, autosomal recessive 28 (OMIM:620375), but with a phenotype in Gen2Phen. PMIDs 37167966; 36745799 report seven HMGCR variants in four unrelated cases. Segregation of the variants and the condition was seen all of the families and in vitro studies revealed that the variant protein had a reduced activity (PMID: 36745799).Created: 22 Aug 2023, 4:37 p.m. | Last Modified: 22 Aug 2023, 4:37 p.m.
Panel Version: 4.22
Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.Created: 22 Aug 2023, 4:30 p.m. | Last Modified: 22 Aug 2023, 4:30 p.m.
Panel Version: 4.22
Julia Baptista (South East Genomic Laboratory Hub, Synnovis, King's College Hospital)
Several families reported and OMIM entry now available.
Morales-Rosado et al. (2023) reported 9 patients from 5 unrelated families with LGMDR28. Symptoms included hypotonia, delayed motor milestones, and axial and neck muscle weakness. Progressive proximal muscle weakness of the upper and lower limbs, waddling gait, muscle atrophy, and increased serum creatine kinase were also described. Biallelic pathogenic variants identified by exome sequencing including missense, in-frame deletion and splice site.
Yogev et al (2023) reported 6 affected members of a large consanguineous Bedouin kindred with LGMDR28. In vitro functional studies of the missense variant supported a partial loss of function effect.
Sources: Expert Review, LiteratureCreated: 21 Aug 2023, 12:50 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Autosomal recessive limb-girdle muscular dystrophy-28; muscle weakness; myopathy
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- NHS GMS
- Phenotypes
-
- Muscular dystrophy, limb-girdle, autosomal recessive 28, OMIM:620375
- OMIM
- 142910
- Clinvar variants
- Variants in HMGCR
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Removed Tag
Achchuthan Shanmugasundram (Genomics England Curator)Tag Q3_23_promote_green was removed from gene: HMGCR.
Added New Source, Added New Source, Status Update
Achchuthan Shanmugasundram (Genomics England Curator)Source NHS GMS was added to HMGCR. Source Expert Review Green was added to HMGCR. Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Removed Tag
Achchuthan Shanmugasundram (Genomics England Curator)Tag Q3_23_MOI was removed from gene: HMGCR.
Added Tag, Added Tag
Sarah Leigh (Genomics England Curator)Tag Q3_23_promote_green tag was added to gene: HMGCR. Tag Q3_23_MOI tag was added to gene: HMGCR.
Entity classified by Genomics England curator
Sarah Leigh (Genomics England Curator)Gene: hmgcr has been classified as Amber List (Moderate Evidence).
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for gene: HMGCR were changed from Autosomal recessive limb-girdle muscular dystrophy-28; muscle weakness; myopathy to Muscular dystrophy, limb-girdle, autosomal recessive 28, OMIM:620375
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Julia Baptista (South East Genomic Laboratory Hub, Synnovis, King's College Hospital)gene: HMGCR was added gene: HMGCR was added to Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies. Sources: Expert Review,Literature Mode of inheritance for gene: HMGCR was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: HMGCR were set to 37167966; 36745799 Phenotypes for gene: HMGCR were set to Autosomal recessive limb-girdle muscular dystrophy-28; muscle weakness; myopathy Review for gene: HMGCR was set to GREEN