DYRK1A - Gene browser

DYRK1A

dual specificity tyrosine phosphorylation regulated kinase 1A

HCNC Approved Symbol: DYRK1A (HGNC:3091)
Genomic Coordinates: 21:37,365,573 - 37,526,358 (21q22.13)
Synonyms: DYRK1, DYRK, MNBH
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

26Patients

In total, 26 patients were diagnosed with a variant in the DYRK1A gene.

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

026
Patient count

Microcephaly: 15 (57.7%)
Patient Count: 15 (57.7%)
% of total patients presenting each phenotype is shown in parentheses.
15 (57.7%)
Delayed speech and language development: 7 (26.9%)
Patient Count: 7 (26.9%)
% of total patients presenting each phenotype is shown in parentheses.
7 (26.9%)
Speech delay: 7 (26.9%)
Patient Count: 7 (26.9%)
% of total patients presenting each phenotype is shown in parentheses.
7 (26.9%)
Global developmental delay: 6 (23.1%)
Patient Count: 6 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
6 (23.1%)
Intellectual disability: 6 (23.1%)
Patient Count: 6 (23.1%)
% of total patients presenting each phenotype is shown in parentheses.
6 (23.1%)