Limb disorders
Gene: ARMC8EnsemblGeneIds (GRCh38): ENSG00000114098
EnsemblGeneIds (GRCh37): ENSG00000114098
ARMC8 is in 1 panel
1 review
Eleanor Williams (Genomics England Curator)
Comment when marking as ready: Rated based on search of literature and OMIMCreated: 16 Oct 2018, 3:11 p.m.
Comment on list classification: No evidence found for an association of this gene with any limb disorder phenotypes.Created: 3 Oct 2018, 12:49 p.m.
ARMC8 is not in OMIM, Gene2Phenotype or Orphanet. Searched also with previous gene symbol of GID5. A PubMed search did not reveal any papers describing and association with limb disorders. Clinvar does not contain any SNPs for this gene.Created: 3 Oct 2018, 12:48 p.m.
Details
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- Phenotypes
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- Polydactyly
- Clinvar variants
- Variants in ARMC8
- Penetrance
- None
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Eleanor Williams (Genomics England Curator)Eleanor Williams: ARMC8 is not in OMIM, Gene2Phe
Entity classified by Genomics England curator
Eleanor Williams (Genomics England Curator)Gene: armc8 has been classified as Red List (Low Evidence).
Entity classified by Genomics England curator
Eleanor Williams (Genomics England Curator)Gene: armc8 has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)ARMC8 was added to Limb disorders panel. Sources: Victorian Clinical Genetics Services
Created
Ellen McDonagh (Genomics England Curator)ARMC8 was created by Ellen McDonagh