GABBR2 - Gene browser

GABBR2

gamma-aminobutyric acid type B receptor subunit 2

HCNC Approved Symbol: GABBR2 (HGNC:4507)
Genomic Coordinates: 9:98,288,109 - 98,708,935 (9q22.33)
Synonyms: HG20, GABABR2, GPRC3B, GPR51
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

5Patients

In total, 5 patients were diagnosed with a variant in the GABBR2 gene.

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

05
Patient count

Autism spectrum disorder: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Speech delay: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Global developmental delay: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Fine motor delay: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Gross motor delay: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)