Genes in panel

Fetal anomalies

Gene: HEY2

Amber List (moderate evidence)

HEY2 (hes related family bHLH transcription factor with YRPW motif 2)
EnsemblGeneIds (GRCh38): ENSG00000135547
EnsemblGeneIds (GRCh37): ENSG00000135547
OMIM: 604674, Gene2Phenotype
HEY2 is in 2 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
OMIM
604674
Clinvar variants
Variants in HEY2
Penetrance
None
Panels with this gene

History Filter Activity

9 Mar 2026, Gel status: 2

Created, Added New Source, Set mode of inheritance

Arina Puzriakova (Genomics England Curator)

gene: HEY2 was added gene: HEY2 was added to Fetal anomalies. Sources: Expert Review Amber Mode of inheritance for gene: HEY2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted