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TK2

thymidine kinase 2

HCNC Approved Symbol
TK2 (HGNC:11831)
Genomic Coordinates
16:66,508,003 - 66,550,291 (16q21)
Synonyms
SCA31
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the TK2 gene.

Frequently observed phenotypes

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

Myopathy
 3 (75.0%)
Insulin resistance
 2 (50.0%)
Ptosis
 2 (50.0%)
Swallowing difficulties
 2 (50.0%)
Abnormality of vision
 1 (25.0%)
TK2 - Gene browser | 3billion