1. Gene
  2. DYRK2 - dual specificity tyrosine phosphorylation regulated kinase 2 Gene

DYRK2 - dual specificity tyrosine phosphorylation regulated kinase 2 Gene

Homo sapiens
Gene ID: 8445 | Gene type: protein coding

About DYRK2

Cytogenetic location: 12q15 Genomic coordinates (GRCh38): 12:67,648,745-67,665,406 (from NCBI)

This gene has 6 transcripts (splice variants), 208 orthologues and 12 paralogues. Ubiquitous expression in colon (RPKM 11.8), small intestine (RPKM 10.4) and 25 other tissues.

Summary

DYRK2 belongs to a family of protein kinases whose members are presumed to be involved in cellular growth and/or development. The family is defined by structural similarity of their kinase domains and their capability to autophosphorylate on tyrosine residues. DYRK2 has demonstrated tyrosine autophosphorylation and catalyzed phosphorylation of histones H3 and H2B in vitro. Two isoforms of DYRK2 have been isolated. The predominant isoform, isoform 1, lacks a 5' terminal insert. [provided by RefSeq, Jul 2008]

DYRK2 Products(3)

mRNA Protein Name
XM_017020032.2 XP_016875521.1 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X1
NM_003583.4 NP_003574.1 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform 1
NM_006482.3 NP_006473.2 dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform 2

DYRK2 Protein Structure

Pkinase

Pkinase: Protein kinase domain (222 - 535)

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  • 601 a.a.
Protein Preferred Names Protein Names

dual specificity tyrosine-phosphorylation-regulated kinase 2

dual specificity tyrosine-(Y)-phosphorylation regulated kinase 2

Related Diseases

Diseases Alias
Waardenburg Syndrome, Type 2b

Waardenburg Syndrome Type 2b

WS2B

Waardenburg Syndrome, Type Iib

Waardenburg Syndrome Type Iib

Intellectual Developmental Disorder, Autosomal Dominant 7

MRD7

Mental Retardation, Autosomal Dominant 7

Autosomal Dominant Non-Syndromic Intellectual Disability 7

Dyrk1a Syndrome

Autosomal Dominant Intellectual Developmental Disorder 7

Autosomal Dominant Mental Retardation 7

Mental Retardation, Autosomal Dominant, Type 7

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus DYRK2 MGD MGI:1330301
Felis catus DYRK2 VGNC VGNC:61687
Bos taurus DYRK2 VGNC VGNC:55902
Rattus norvegicus DYRK2 RGD RGD:1312039
Macaca mulatta DYRK2 VGNC VGNC:72018
Canis familiaris DYRK2 VGNC VGNC:40157
Others DYRK2 NCBI