SATB2 - Gene browser

SATB2

SATB homeobox 2

HCNC Approved Symbol: SATB2 (HGNC:21637)
Genomic Coordinates: 2:199,269,500 - 199,471,266 (2q33.1)
Synonyms: KIAA1034, FLJ21474
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

16Patients

In total, 16 patients were diagnosed with a variant in the SATB2 gene.

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

016
Patient count

Intellectual disability: 6 (37.5%)
Patient Count: 6 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
6 (37.5%)
Global developmental delay: 5 (31.3%)
Patient Count: 5 (31.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (31.3%)
Developmental delay: 4 (25.0%)
Patient Count: 4 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (25.0%)
Strabismus: 3 (18.8%)
Patient Count: 3 (18.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (18.8%)
Facial dysmorphism: 3 (18.8%)
Patient Count: 3 (18.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (18.8%)