LRSAM1 - Gene browser

LRSAM1

leucine rich repeat and sterile alpha motif containing 1

HCNC Approved Symbol: LRSAM1 (HGNC:25135)
Genomic Coordinates: 9:127,451,486 - 127,503,501 (9q33.3-q34.11)
Synonyms: FLJ31641, CMT2P, RIFLE, TAL
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

2Patients

In total, 2 patients were diagnosed with a variant in the LRSAM1 gene.

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

02
Patient count

Axonal neuropathy: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Myotonia: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Weakness in lower extremities: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Peripheral neuropathy, sensory: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)