GNB1 - Gene browser

GNB1

G protein subunit beta 1

HCNC Approved Symbol: GNB1 (HGNC:4396)
Genomic Coordinates: 1:1,785,286 - 1,891,087 (1p36.33)
Synonyms
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

21Patients

In total, 21 patients were diagnosed with a variant in the GNB1 gene.

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

021
Patient count

Developmental delay: 4 (19.0%)
Patient Count: 4 (19.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (19.0%)
Speech delay: 4 (19.0%)
Patient Count: 4 (19.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (19.0%)
Hypotonia: 4 (19.0%)
Patient Count: 4 (19.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (19.0%)
Global developmental delay: 4 (19.0%)
Patient Count: 4 (19.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (19.0%)
Delayed development: 3 (14.3%)
Patient Count: 3 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (14.3%)