STX1B - Gene browser | 3billion

STX1B

STX1B

syntaxin 1B

HCNC Approved Symbol: STX1B (HGNC:18539)
Genomic Coordinates: 16:30,989,256 - 31,010,638 (16p11.2)
Synonyms: STX1B1, STX1B2
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 STX1B 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

Epilepsy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Global developmental delay: 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

STX1B - Gene browser | 3billion