TLK2 - Gene browser

TLK2

tousled like kinase 2

HCNC Approved Symbol: TLK2 (HGNC:11842)
Genomic Coordinates: 17:62,470,914 - 62,615,481 (17q23.2)
Synonyms: PKU-ALPHA, MGC44450
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

19Patients

In total, 19 patients were diagnosed with a variant in the TLK2 gene.

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

019
Patient count

Global developmental delay: 8 (42.1%)
Patient Count: 8 (42.1%)
% of total patients presenting each phenotype is shown in parentheses.
8 (42.1%)
Intellectual disability: 7 (36.8%)
Patient Count: 7 (36.8%)
% of total patients presenting each phenotype is shown in parentheses.
7 (36.8%)
Hypertelorism: 4 (21.1%)
Patient Count: 4 (21.1%)
% of total patients presenting each phenotype is shown in parentheses.
4 (21.1%)
Microcephaly: 3 (15.8%)
Patient Count: 3 (15.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.8%)
Delayed speech and language development: 3 (15.8%)
Patient Count: 3 (15.8%)
% of total patients presenting each phenotype is shown in parentheses.
3 (15.8%)