Gene Gene information from NCBI Gene database.
Entrez ID 8444
Gene name Dual specificity tyrosine phosphorylation regulated kinase 3
Gene symbol DYRK3
Synonyms (NCBI Gene)
DYRK5REDREDKhYAK3-2
Chromosome 1
Chromosome location 1q32.1
Summary This gene product belongs to the DYRK family of dual-specificity protein kinases that catalyze autophosphorylation on serine/threonine and tyrosine residues. The members of this family share structural similarity, however, differ in their substrate specif
miRNA miRNA information provided by mirtarbase database.
122
miRTarBase ID miRNA Experiments Reference
MIRT029437 hsa-miR-26b-5p Microarray 19088304
MIRT710186 hsa-miR-3646 HITS-CLIP 19536157
MIRT710185 hsa-miR-1252-3p HITS-CLIP 19536157
MIRT710184 hsa-miR-4318 HITS-CLIP 19536157
MIRT710183 hsa-miR-7114-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
50
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000242 Component Pericentriolar material IDA 29973724
GO:0000287 Function Magnesium ion binding IDA 10779429
GO:0000287 Function Magnesium ion binding IEA
GO:0004672 Function Protein kinase activity IDA 10779429
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603497 3094 ENSG00000143479
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43781
Protein name Dual specificity tyrosine-phosphorylation-regulated kinase 3 (EC 2.7.12.1) (Regulatory erythroid kinase) (REDK)
Protein function Dual-specificity protein kinase that promotes disassembly of several types of membraneless organelles during mitosis, such as stress granules, nuclear speckles and pericentriolar material (PubMed:29973724). Dual-specificity tyrosine-regulated ki
PDB 5Y86
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 209 522 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1: Highly expressed in testis and in hematopoietic tissue such as fetal liver, and bone marrow (PubMed:10779429). Isoform 1: Predominant form in fetal liver and bone marrow (PubMed:10779429). Isoform 1: Present at low levels in
Sequence
MGGTARGPGRKDAGPPGAGLPPQQRRLGDGVYDTFMMIDETKCPPCSNVLCNPSEPPPPR
RLNMTTEQFTGDHTQHFLDGGEMKVEQLFQEFGNRKSNTIQSDGISDSEKCSPTVSQGKS
SDCLNTVKSNSSSKAPKVVPLTPEQALKQYKHHLTAYEKLEIINYPEIYFVGPNAKKRHG
VIGGPNNGGYDDADGAYIHVPRDHLAYRYEVLKIIGKGSFGQVARVYDHKLRQYVALKMV
RNEKRFHRQAAEEIRILEHLKKQDKTGSMNVIHMLESFTFRNHVCMAFELLSIDLYELIK
KNKFQGFSVQLVRKFAQSILQSLDALHKNKIIHCDLKPENILLKHHGRSSTKVIDFGSSC
FEYQKLYTYIQSRFYRAPEIILGSRYSTPIDIWSFGCILAELLTGQPLFPGEDEGDQLAC
MMELLGMPPPKLLEQSKRAKYFINSKGIPRYCSVTTQADGRVVLVGGRSRRGKKRGPPGS
KDWGTALKGCDDYLFIEFLKRCLHWDPSARLTPAQALRHPWI
SKSVPRPLTTIDKVSGKR
VVNPASAFQGLGSKLPPVVGIANKLKANLMSETNGSIPLCSVLPKLIS
Sequence length 588
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
MIGRAINE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 1 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Anemia Anemia BEFREE 29634919
★☆☆☆☆
Found in Text Mining only
Anorexia Anorexia BEFREE 31684854
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 24376576 Associate
★☆☆☆☆
Found in Text Mining only
Color blindness Color Blindness BEFREE 12626747
★☆☆☆☆
Found in Text Mining only
Craniofacial Dysostosis Craniofacial Dysostosis BEFREE 30642732
★☆☆☆☆
Found in Text Mining only
Craniofacial dysostosis type 1 Craniofacial Dysostosis BEFREE 30642732
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 28611698
★☆☆☆☆
Found in Text Mining only
Eating Disorders Eating Disorders BEFREE 31684854
★☆☆☆☆
Found in Text Mining only
Hereditary Autosomal Dominant Spastic Paraplegia Spastic paraplegia BEFREE 10493830
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 31066068
★☆☆☆☆
Found in Text Mining only