LAMA2 - Gene browser

LAMA2

laminin subunit alpha 2

HCNC Approved Symbol: LAMA2 (HGNC:6482)
Genomic Coordinates: 6:128,883,138 - 129,516,566 (6q22.33)
Synonyms: LAMM
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

43Patients

In total, 43 patients were diagnosed with a variant in the LAMA2 gene.

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

043
Patient count

Hypotonia: 11 (25.6%)
Patient Count: 11 (25.6%)
% of total patients presenting each phenotype is shown in parentheses.
11 (25.6%)
Muscle weakness: 8 (18.6%)
Patient Count: 8 (18.6%)
% of total patients presenting each phenotype is shown in parentheses.
8 (18.6%)
Elevated creatine kinase: 8 (18.6%)
Patient Count: 8 (18.6%)
% of total patients presenting each phenotype is shown in parentheses.
8 (18.6%)
Generalized hypotonia: 5 (11.6%)
Patient Count: 5 (11.6%)
% of total patients presenting each phenotype is shown in parentheses.
5 (11.6%)
Myopathy: 5 (11.6%)
Patient Count: 5 (11.6%)
% of total patients presenting each phenotype is shown in parentheses.
5 (11.6%)