ALX3 - Gene browser | 3billion

ALX3

ALX3

ALX homeobox 3

HCNC Approved Symbol: ALX3 (HGNC:449)
Genomic Coordinates: 1:110,059,870 - 110,070,672 (1p13.3)
Synonyms: FND
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ALX3 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Cleft lip/palate: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Facial dysmorphism: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

ALX3 - Gene browser | 3billion