Homo sapiens Gene: DYRK1A
Summary
InnateDB Gene IDBG-3163.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DYRK1A
Gene Name dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
Synonyms DYRK; DYRK1; HP86; MNB; MNBH; MRD7
Species Homo sapiens
Ensembl Gene ENSG00000157540
Encoded Proteins
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5' UTR or in the 3' coding region. These variants encode at least five different isoforms. [provided by RefSeq, Jul 2008]
This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5\' UTR or in the 3\' coding region. These variants encode at least five different isoforms. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 21:37365790-37517450
Strand Forward strand
Band q22.13
Transcripts
ENST00000339659 ENSP00000340373
ENST00000338785 ENSP00000342690
ENST00000398960 ENSP00000381932
ENST00000398956 ENSP00000381929
ENST00000426672 ENSP00000412269
ENST00000455097 ENSP00000398483
ENST00000462274
ENST00000498351
ENST00000608928
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 71 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 71 [view]
Protein-Protein 70 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0004712 protein serine/threonine/tyrosine kinase activity
GO:0004713 protein tyrosine kinase activity
GO:0004715 non-membrane spanning protein tyrosine kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
GO:0042802 identical protein binding
GO:0043621 protein self-association
GO:0048156 tau protein binding
Biological Process
GO:0000278 mitotic cell cycle
GO:0000381 regulation of alternative mRNA splicing, via spliceosome
GO:0006468 protein phosphorylation
GO:0007399 nervous system development
GO:0007623 circadian rhythm
GO:0018105 peptidyl-serine phosphorylation
GO:0018107 peptidyl-threonine phosphorylation
GO:0018108 peptidyl-tyrosine phosphorylation
GO:0043518 negative regulation of DNA damage response, signal transduction by p53 class mediator
GO:0046777 protein autophosphorylation
GO:0090312 positive regulation of protein deacetylation
Cellular Component
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0016607 nuclear speck
GO:0030529 ribonucleoprotein complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
EGFR1 pathway
Hedgehog pathway
TCR pathway
REACTOME
G0 and Early G1 pathway
Mitotic G1-G1/S phases pathway
Cell Cycle pathway
Cell Cycle, Mitotic pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.368240 Hs.719974
RefSeq NM_001396 NM_101395 NM_130436 NM_130438 XM_005260931 XM_005260933 XM_006723976 XM_006723977 XM_006723978 XM_006723979
HUGO
OMIM
CCDS CCDS13653 CCDS13654 CCDS42925 CCDS42926
HPRD 09018
IMGT
EMBL
GenPept
RNA Seq Atlas