Cerebral vascular malformations
Gene: RELNEnsemblGeneIds (GRCh38): ENSG00000189056
EnsemblGeneIds (GRCh37): ENSG00000189056
OMIM: 600514, Gene2Phenotype
RELN is in 16 panels
1 review
Alice Gardham (Genomics England)
Comment when marking as ready: Not associated with cerebral vascular malformationsCreated: 12 Dec 2016, 11:45 a.m.
Not associated with cerebral vascular malformationsCreated: 12 Dec 2016, 11:45 a.m.
Details
- Sources
-
- Yorkshire and North East GLH
- NHS GMS
- Expert Review Red
- UKGTN
- Phenotypes
-
- Cerebral Malformation Disorders
- OMIM
- 600514
- Clinvar variants
- Variants in RELN
- Penetrance
- Complete
- Panels with this gene
-
- Intellectual disability
- Early onset or syndromic epilepsy
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Cerebellar hypoplasia
- Inherited white matter disorders
- Adult onset neurodegenerative disorder
- Familial Hirschsprung Disease
- Cerebral vascular malformations
- Malformations of cortical development
- Ataxia and cerebellar anomalies - narrow panel
- Hereditary ataxia with onset in adulthood
- White matter disorders and cerebral calcification - narrow panel
- Hereditary ataxia
- Fetal anomalies
- Primary immunodeficiency or monogenic inflammatory bowel disease
History Filter Activity
Added New Source
Louise Daugherty (Genomics England Curator)Source Yorkshire and North East GLH was added to RELN.
Added New Source
Louise Daugherty (Genomics England Curator)Source NHS GMS was added to RELN.
panel promoted to version 1
Alice Gardham (Genomics England)Promoted to version 1 on the 19th December 2016
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)RELN was added to Cerebrovascular disorderspanel. Sources: UKGTN
Created
Ellen McDonagh (Genomics England Curator)RELN was created by ellenmcdonagh