SELENON - Gene browser

SELENON

selenoprotein N

HCNC Approved Symbol: SELENON (HGNC:15999)
Genomic Coordinates: 1:25,800,193 - 25,818,221 (1p36.11)
Synonyms: SELN, RSS, RSMD1, MDRS1, SEPN1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

10Patients

In total, 10 patients were diagnosed with a variant in the SELENON gene.

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

010
Patient count

Scoliosis: 5 (50.0%)
Patient Count: 5 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (50.0%)
Emg: myopathy: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)
Proximal muscle weakness: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)
Muscle weakness: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)
Generalized hypotonia: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)