ARID1B - Gene browser

ARID1B

AT-rich interaction domain 1B

HCNC Approved Symbol: ARID1B (HGNC:18040)
Genomic Coordinates: 6:156,776,026 - 157,210,779 (6q25.3)
Synonyms: KIAA1235, ELD/OSA1, p250R, BAF250b, DAN15, 6A3-5, SMARCF2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

75Patients

In total, 75 patients were diagnosed with a variant in the ARID1B gene.

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

075
Patient count

Global developmental delay: 18 (24.0%)
Patient Count: 18 (24.0%)
% of total patients presenting each phenotype is shown in parentheses.
18 (24.0%)
Global development delay: 15 (20.0%)
Patient Count: 15 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
15 (20.0%)
Failure to thrive: 12 (16.0%)
Patient Count: 12 (16.0%)
% of total patients presenting each phenotype is shown in parentheses.
12 (16.0%)
Developmental delay: 11 (14.7%)
Patient Count: 11 (14.7%)
% of total patients presenting each phenotype is shown in parentheses.
11 (14.7%)
Long eyelashes: 11 (14.7%)
Patient Count: 11 (14.7%)
% of total patients presenting each phenotype is shown in parentheses.
11 (14.7%)