1. Gene
  2. DCLK2 - doublecortin like kinase 2 Gene

DCLK2 - doublecortin like kinase 2 Gene

Homo sapiens

Also known as CL2; DCK2; CLIK2; DCDC3; CLICK2; DCDC3B; DCAMKL2; CLICK-II

Gene ID: 166614 | Gene type: protein coding

About DCLK2

Cytogenetic location: 4q31.23-q31.3 Genomic coordinates (GRCh38): 4:150,078,445-150,257,438 (from NCBI)

This gene has 7 transcripts (splice variants), 353 orthologues and 22 paralogues. Biased expression in brain (RPKM 21.2), heart (RPKM 3.5) and 9 other tissues.

Summary

This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. Mouse studies show that the DCX gene, another family member, and this gene share function in the establishment of hippocampal organization and that their absence results in a severe epileptic phenotype and lethality, as described in human patients with lissencephaly. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Sep 2010]

DCLK2 Products(3)

mRNA Protein Name
NM_001040260.4 NP_001035350.2 serine/threonine-protein kinase DCLK2 isoform a
NM_001040261.5 NP_001035351.4 serine/threonine-protein kinase DCLK2 isoform b
NM_001410852.1 NP_001397781.1 serine/threonine-protein kinase DCLK2 isoform c
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32707033 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

DCLK2 Protein Structure

DCX

DCX: Doublecortin (89 - 153)

DCX

DCX: Doublecortin (214 - 275)

Pkinase

Pkinase: Protein kinase domain (394 - 651)

  • 0
  • 200
  • 400
  • 600
  • 766 a.a.
Protein Preferred Names Protein Names

serine/threonine-protein kinase DCLK2

CaMK-like CREB regulatory kinase 2

DCLK2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
DCLK2 Q8N568 KLHL15 Homo sapiens Q96M94
Anti Tag CoIP
33199366
Intra
DCLK2 Q8N568 YWHAE Homo sapiens P62258
Crosslink
36931259
Intra
DCLK2 Q8N568 YWHAE Homo sapiens P62258
Pull Down
32707033
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Lissencephaly

Pachygyria

Broad Gyri Of Cerebrum

Large Gyri Of Cerebrum

Macrogyria

Band Heterotopia

Subcortical Band Heterotopia

Double Cortex Syndrome

Subcortical Laminar Heterotopia

Double Cortex

Band Heterotopia Of Brain

BH

Heco

Heterotopic Cortex

Familial Band Heterotopia

Dc

Dc Syndrome

Heterotopia, Subcortical Band

Sbh

Sclh

Bhy

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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
Bos taurus DCLK2 VGNC VGNC:27915
Felis catus DCLK2 VGNC VGNC:61368
Canis familiaris DCLK2 VGNC VGNC:39804
Mus musculus DCLK2 MGD MGI:1918012
Rattus norvegicus DCLK2 RGD RGD:1308384
Macaca mulatta DCLK2 VGNC VGNC:71670
Others DCLK2 NCBI