Genes in panel

Early onset or syndromic epilepsy

Gene: ADGRL1

Amber List (moderate evidence)

ADGRL1 (adhesion G protein-coupled receptor L1)
EnsemblGeneIds (GRCh38): ENSG00000072071
EnsemblGeneIds (GRCh37): ENSG00000072071
OMIM: 616416, Gene2Phenotype
ADGRL1 is in 2 panels

1 review

Achchuthan Shanmugasundram (Genomics England Curator)

I don't know

PMID:35907405 reported the identification of monoallelic ADGRL1 variants in ten individuals with a neurodevelopmental disorder comprising developmental delay, intellectual disability, attention deficit hyperactivity and autism spectrum disorders, and epilepsy. This includes a case that was previously reported in PMID:30504930. Epilepsy was reported in two of these cases. This gene has been associated with relevant phenotype in OMIM (MIM #620065), but not yet in Gene2Phenotype.
Sources: Literature
Created: 26 Jun 2024, 5:36 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065
OMIM
616416
Clinvar variants
Variants in ADGRL1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

26 Jun 2024, Gel status: 2

Entity classified by Genomics England curator

Achchuthan Shanmugasundram (Genomics England Curator)

Gene: adgrl1 has been classified as Amber List (Moderate Evidence).

26 Jun 2024, Gel status: 2

Entity classified by Genomics England curator

Achchuthan Shanmugasundram (Genomics England Curator)

Gene: adgrl1 has been classified as Amber List (Moderate Evidence).

26 Jun 2024, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Achchuthan Shanmugasundram (Genomics England Curator)

gene: ADGRL1 was added gene: ADGRL1 was added to Early onset or syndromic epilepsy. Sources: Literature Mode of inheritance for gene: ADGRL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ADGRL1 were set to 35907405 Phenotypes for gene: ADGRL1 were set to Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065 Review for gene: ADGRL1 was set to AMBER