LAMB2 - Gene browser

LAMB2

laminin subunit beta 2

HCNC Approved Symbol: LAMB2 (HGNC:6487)
Genomic Coordinates: 3:49,121,114 - 49,133,050 (3p21.31)
Synonyms: NPHS5, LAMS
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

7Patients

In total, 7 patients were diagnosed with a variant in the LAMB2 gene.

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

07
Patient count

Congenital nephrotic syndrome: 5 (71.4%)
Patient Count: 5 (71.4%)
% of total patients presenting each phenotype is shown in parentheses.
5 (71.4%)
Infantile death: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Absence of renal corticomedullary differentiation: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Edema: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)
Enlarged kidney: 2 (28.6%)
Patient Count: 2 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
2 (28.6%)