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DYRK1A - dual specificity tyrosine phosphorylation regulated kinase 1A
- Synonym(s) :
- Previous symbols and names : DYRK, DYRK1, MNBH, dual specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
- Type : gene with protein product
- Chromosomal location : 21q22.13
- OMIM: 600855
- HGNC: 3091
- UniProtKB: Q13627
- Genatlas: DYRK1A
- Ensembl: ENSG00000157540
- IUPHAR-DB: 2009
- Reactome: Q13627
- LOVD: DYRK1A
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Intellectual disability syndrome due to a DYRK1A point mutation
ORPHA:464311 
- Role in the phenotype of DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
ORPHA:268261
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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