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
-
- Cerebellar hypoplasia
- Malformations of cortical development
- Adult onset neurodegenerative disorder
- Hereditary ataxia with onset in adulthood
- Ataxia and cerebellar anomalies - narrow panel
- White matter disorders and cerebral calcification - narrow panel
- Childhood onset dystonia, chorea or related movement disorder
- Inherited white matter disorders
- Hereditary ataxia
- Familial Hirschsprung Disease
- Intellectual disability
- DDG2P
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Cerebral vascular malformations
- Early onset or syndromic epilepsy
- Fetal anomalies
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