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Fetal anomalies

Gene: ELMO2

Amber List (moderate evidence)

ELMO2 (engulfment and cell motility 2)
EnsemblGeneIds (GRCh38): ENSG00000062598
EnsemblGeneIds (GRCh37): ENSG00000062598
OMIM: 606421, Gene2Phenotype
ELMO2 is in 2 panels

1 review

Rebecca Foulger (Genomics England curator)

I don't know

DDG2P rating in original PAGE list: Probable for Intraosseous Vascular Malformation
Created: 11 Dec 2018, 9:04 a.m.


Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
  • Intraosseous Vascular Malformation
Clinvar variants
Variants in ELMO2
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: ELMO2 was added gene: ELMO2 was added to Fetal anomalies. Sources: PAGE DD-Gene2Phenotype,Expert Review Amber Mode of inheritance for gene: ELMO2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ELMO2 were set to Intraosseous Vascular Malformation