Stroke
Gene: PDCD10EnsemblGeneIds (GRCh38): ENSG00000114209
EnsemblGeneIds (GRCh37): ENSG00000114209
OMIM: 609118, Gene2Phenotype
PDCD10 is in 6 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
At least 7 families reported and stroke can be a feature of the condition.
Sources: LiteratureCreated: 12 May 2020, 5:25 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cerebral cavernous malformations 3 MIM#603285
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Cerebral cavernous malformations 3 MIM#603285
- OMIM
- 609118
- Clinvar variants
- Variants in PDCD10
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: pdcd10 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: pdcd10 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: PDCD10 was added gene: PDCD10 was added to Stroke. Sources: Literature Mode of inheritance for gene: PDCD10 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PDCD10 were set to 30356112; 15543491 Phenotypes for gene: PDCD10 were set to Cerebral cavernous malformations 3 MIM#603285 Review for gene: PDCD10 was set to GREEN