ALX1 - Gene browser | 3billion

ALX1

ALX1

ALX homeobox 1

HCNC Approved Symbol: ALX1 (HGNC:1494)
Genomic Coordinates: 12:85,280,220 - 85,301,784 (12q21.31)
Synonyms: CART1
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 ALX1 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

Clinical anophthalmia, unilateral/bilateral: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Intrauterine growth retardation: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Patent ductus arteriosus: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Unilateral microphthalmos: 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

ALX1 - Gene browser | 3billion