1. Gene
  2. DCLK1 - doublecortin like kinase 1 Gene

DCLK1 - doublecortin like kinase 1 Gene

Homo sapiens

Also known as CL1; DCLK; CLICK1; DCDC3A; DCAMKL1

Gene ID: 9201 | Gene type: protein coding

About DCLK1

Cytogenetic location: 13q13.3 Genomic coordinates (GRCh38): 13:35,768,652-36,131,939 (from NCBI)

This gene has 8 transcripts (splice variants), 282 orthologues and 22 paralogues. Biased expression in brain (RPKM 28.5), fat (RPKM 4.0) and 7 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. The encoded protein is involved in several different cellular processes, including neuronal migration, retrograde transport, neuronal Apoptosis and neurogenesis. This gene is up-regulated by brain-derived neurotrophic factor and associated with memory and general cognitive abilities. Multiple transcript variants generated by two alternative promoter usage and alternative splicing have been reported, but the full-length nature and biological validity of some variants have not been defined. These variants encode different isoforms, which are differentially expressed and have different kinase activities.[provided by RefSeq, Sep 2010]

DCLK1 Products(6)

mRNA Protein Name
NM_001195415.2 NP_001182344.1 serine/threonine-protein kinase DCLK1 isoform 2
NM_001195416.2 NP_001182345.1 serine/threonine-protein kinase DCLK1 isoform 3
NM_001195430.2 NP_001182359.1 serine/threonine-protein kinase DCLK1 isoform 4
NM_001330071.2 NP_001317000.1 serine/threonine-protein kinase DCLK1 isoform 5
NM_001330072.2 NP_001317001.1 serine/threonine-protein kinase DCLK1 isoform 5
NM_004734.5 NP_004725.1 serine/threonine-protein kinase DCLK1 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Reference Source
involved in response to virus IEP
IEP: Inferred from expression pattern
16548883 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

DCLK1 Protein Structure

DCX

DCX: Doublecortin (74 - 138)

DCX

DCX: Doublecortin (203 - 264)

Pkinase

Pkinase: Protein kinase domain (390 - 647)

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

serine/threonine-protein kinase DCLK1

doublecortin domain-containing protein 3A

Recombinant DCLK1 Proteins

Cat. No. Product Name Accession Purity
HY-P75307 DCLK1 Protein, Human (sf9, His-GST) O15075-1 (M1-V705) ≥95%
HY-P75308 DCLK1 Protein, Human (sf9) O15075-1 (M1-V705) ≥95%

Related Diseases

Diseases Alias
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

Zellweger Syndrome

Cerebrohepatorenal Syndrome

Zellweger Leukodystrophy

Zs

Congenital Iron Overload

Chr

Zws

Severe Pbd-Zsd

Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Colonic Benign Neoplasm

Colon Neoplasm

Colonic Mass

Colonic Tumor

Neoplasm Of Colon

Neoplasm Of The Colon

Colonic Neoplasms

Colon Cancer

Colon Carcinoma Nos

Colonic Cancer

Metastatic Colon Cancer Nos

Lymphangioma

Lymphatic Malformation

Lymphatic Malformations

Benign Lymphangioma

Congenital Lymphangioma

Lymphangiomas

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
Canis familiaris DCLK1 VGNC VGNC:39803
Felis catus DCLK1 VGNC VGNC:61367
Mus musculus DCLK1 MGD MGI:1330861
Rattus norvegicus DCLK1 RGD RGD:68437
Macaca mulatta DCLK1 VGNC VGNC:71745
Others DCLK1 NCBI