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Fetal anomalies

Gene: ARFGEF2

Amber List (moderate evidence)

ARFGEF2 (ADP ribosylation factor guanine nucleotide exchange factor 2)
EnsemblGeneIds (GRCh38): ENSG00000124198
EnsemblGeneIds (GRCh37): ENSG00000124198
OMIM: 605371, Gene2Phenotype
ARFGEF2 is in 6 panels

1 review

Rebecca Foulger (Genomics England curator)

I don't know

DDG2P rating in original PAGE list: Probable for PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY
Created: 11 Dec 2018, 9:04 a.m.

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
Phenotypes
  • PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY
OMIM
605371
Clinvar variants
Variants in ARFGEF2
Penetrance
None
Panels with this gene

History Filter Activity

8 Nov 2018, Gel status: 2

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

Rebecca Foulger (Genomics England curator)

gene: ARFGEF2 was added gene: ARFGEF2 was added to Fetal anomalies. Sources: PAGE DD-Gene2Phenotype,Expert Review Amber Mode of inheritance for gene: ARFGEF2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ARFGEF2 were set to PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY