CPLX1 - Gene browser | 3billion

CPLX1

CPLX1

complexin 1

HCNC Approved Symbol: CPLX1 (HGNC:2309)
Genomic Coordinates: 4:784,957 - 826,129 (4p16.3)
Synonyms: CPX-I
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 CPLX1 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

Delayed development: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Focal seizures: 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

CPLX1 - Gene browser | 3billion