ALX4 - Gene browser | 3billion

ALX4

ALX4

ALX homeobox 4

HCNC Approved Symbol: ALX4 (HGNC:450)
Genomic Coordinates: 11:44,260,440 - 44,310,139 (11p11.2)
Synonyms: FPP, PFM, KIAA1788, PFM2
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ALX4 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

Coronal synostosis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Global developmental delay: 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

ALX4 - Gene browser | 3billion