Pain syndromes
Gene: DSTEnsemblGeneIds (GRCh38): ENSG00000151914
EnsemblGeneIds (GRCh37): ENSG00000151914
OMIM: 113810, Gene2Phenotype
DST is in 5 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
At least 4 unrelated families reported with pain insensitivity as a feature of the condition.
Sources: OtherCreated: 4 Mar 2021, 12:31 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neuropathy, hereditary sensory and autonomic, type VI MIM#614653
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Other
- Phenotypes
-
- Neuropathy, hereditary sensory and autonomic, type VI MIM#614653
- OMIM
- 113810
- Clinvar variants
- Variants in DST
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: dst has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: dst has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: DST was added gene: DST was added to Pain syndromes. Sources: Other Mode of inheritance for gene: DST was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DST were set to 28468842; 32528525; 22522446; 30371979 Phenotypes for gene: DST were set to Neuropathy, hereditary sensory and autonomic, type VI MIM#614653 Review for gene: DST was set to GREEN gene: DST was marked as current diagnostic