FKTN - Gene browser

FKTN

fukutin

HCNC Approved Symbol: FKTN (HGNC:3622)
Genomic Coordinates: 9:105,558,130 - 105,641,118 (9q31.2)
Synonyms: LGMD2M, FCMD
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

3Patients

In total, 3 patients were diagnosed with a variant in the FKTN gene.

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

03
Patient count

Cerebellar cyst: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Elevated serum creatine kinase: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Gray matter heterotopia: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Infantile muscular hypotonia: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Seizure: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)