LMNB2 - Gene browser

LMNB2

lamin B2

HCNC Approved Symbol: LMNB2 (HGNC:6638)
Genomic Coordinates: 19:2,428,166 - 2,456,959 (19p13.3)
Synonyms: LMN2
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the LMNB2 gene.

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

01
Patient count

Dystonia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Epilepsy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypertonia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Intellectual disability: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Myoclonus: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)