SH3BP2 - Gene browser | 3billion

SH3BP2

SH3BP2

SH3 domain binding protein 2

HCNC Approved Symbol: SH3BP2 (HGNC:10825)
Genomic Coordinates: 4:2,793,085 - 2,841,096 (4p16.3)
Synonyms: RES4-23, CRBM
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 SH3BP2 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

Fibrous dysplasia of the bones: 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

SH3BP2 - Gene browser | 3billion