HEY2 - Gene browser

HEY2

hes related family bHLH transcription factor with YRPW motif 2

HCNC Approved Symbol: HEY2 (HGNC:4881)
Genomic Coordinates: 6:125,749,632 - 125,761,269 (6q22.31)
Synonyms: bHLHb32, HERP1, HESR2
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.

Diagnosed Cases

5Patients

In total, 5 patients were diagnosed with a variant in the HEY2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

05
Patient count

Ventricular septal defect: 4 (80.0%)
Patient Count: 4 (80.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (80.0%)
Dextrocardia: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Transposition of the great arteries: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Asplenia: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Situs inversus totalis: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)