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

DCLK1 - doublecortin like kinase 1 Gene

中文名称:双皮质素样激酶 1

种属: Homo sapiens

同用名: CL1; DCLK; CLICK1; DCDC3A; DCAMKL1

基因 ID: 9201 | 基因类型: protein coding

关于 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.

功能概要

该基因编码蛋白激酶超家族和双皮质素家族的成员。该基因编码的蛋白质包含两个 N 端双皮质素结构域,可结合微管并调节微管聚合,一个 C 端丝氨酸/苏氨酸蛋白激酶结构域,与 Ca2+/钙调蛋白依赖性蛋白激酶具有显着同源性,以及一个丝氨酸/双皮质素和蛋白激酶结构域之间富含脯氨酸的结构域,介导多种蛋白质-蛋白质相互作用。编码蛋白的微管聚合活性与其蛋白激酶活性无关。编码的蛋白质参与几种不同的细胞过程,包括神经元迁移、逆行运输、神经元凋亡和神经发生。该基因受脑源性神经营养因子上调,并与记忆和一般认知能力相关。已经报道了由两个替代启动子使用和替代剪接产生的多个转录变体,但尚未定义某些变体的全长性质和生物学有效性。这些变体编码不同的同种型,它们的表达方式不同并且具有不同的激酶活性。[RefSeq 提供,2010 年 9 月]

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 基因产物(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
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in response to virus IEP
IEP: 通过表达模式推断
16548883 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

DCLK1 蛋白结构

DCX

DCX: Doublecortin (74 - 138)

DCX

DCX: Doublecortin (203 - 264)

Pkinase

Pkinase: Protein kinase domain (390 - 647)

  • 0
  • 200
  • 400
  • 600
  • 740 a.a.
蛋白主名 其他名称

serine/threonine-protein kinase DCLK1

doublecortin domain-containing protein 3A

重组 DCLK1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P75307 DCLK1 Protein, Human (sf9, His-GST) O15075-1 (M1-V705) ≥95%
HY-P75308 DCLK1 Protein, Human (sf9) O15075-1 (M1-V705) ≥95%

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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