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CDKL5 Gene

protein-coding   GIFtS: 65
GCID: GC0XP018443

Cyclin-Dependent Kinase-Like 5

(Previous name: serine/threonine kinase 9)
(Previous symbol: STK9)
  See CDKL5-related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Cyclin-Dependent Kinase-Like 51 2     EIEE22 5
STK91 2 3 5     ISSX2 5
Serine/Threonine Kinase 91 2     Cyclin Dependent Kinase 5 Transcript2
Serine/Threonine-Protein Kinase 92 3     EC 2.7.118
EC 2.7.11.223 8     

External Ids:    HGNC: 114111   Entrez Gene: 67922   Ensembl: ENSG000000080867   OMIM: 3002035   UniProtKB: O760393   

Export aliases for CDKL5 gene to outside databases

Previous GC identifers: GC0XP017109 GC0XP017645 GC0XP017805 GC0XP018203 GC0XP018353 GC0XP016199


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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Entrez Gene summary for CDKL5 Gene:
This gene is a member of Ser/Thr protein kinase family and encodes a phosphorylated protein with protein kinase
activity. Mutations in this gene have been associated with X-linked infantile spasm syndrome (ISSX), also known
as X-linked West syndrome, and Rett syndrome (RTT). Alternate transcriptional splice variants have been
characterized. (provided by RefSeq, Jul 2008)

GeneCards Summary for CDKL5 Gene:
CDKL5 (cyclin-dependent kinase-like 5) is a protein-coding gene. Diseases associated with CDKL5 include epileptic encephalopathy, early infantile, 2, and cdkl5-related angelman-like syndrome. GO annotations related to this gene include protein serine/threonine kinase activity and kinase activity. An important paralog of this gene is CDKL1.

UniProtKB/Swiss-Prot: CDKL5_HUMAN, O76039
Function: Mediates phosphorylation of MECP2

Gene Wiki entry for CDKL5 Gene


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence at NCBI GenBank:
NC_000023.10  NT_167197.2  NC_018934.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the CDKL5 gene promoter:
         Sox5   HFH-1   Cart-1   FOXD3   Hlf   FOXL1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidCDKL5 promoter sequence
   Search Chromatin IP Primers for CDKL5

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat CDKL5


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: Xp22   Ensembl cytogenetic band:  Xp22.13   HGNC cytogenetic band: Xp22

CDKL5 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
CDKL5 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XP018443:  view genomic region     (about GC identifiers)

Start:
18,443,703 bp from pter      End:
18,671,749 bp from pter
Size:
228,047 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, Cloud-Clone Corp., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: CDKL5_HUMAN, O76039 (See protein sequence)
Recommended Name: Cyclin-dependent kinase-like 5  
Size: 1030 amino acids; 115538 Da
Subunit: Interacts with MECP2
Caution: It is uncertain whether Met-1 or Met-10 is the initiator
Sequence caution: Sequence=CAA61445.1; Type=Frameshift; Positions=415;
1 PDB 3D structure from and Proteopedia for CDKL5:
4BGQ (3D)    
Secondary accessions: G9B9X4 Q14198 Q5H985 Q8IYC7 Q9UJL6
Alternative splicing: 2 isoforms:  O76039-1   O76039-2   (Predominant transcript in brain)

Explore the universe of human proteins at neXtProt for CDKL5: NX_O76039

Explore proteomics data for CDKL5 at MOPED

Post-translational modifications: 

  • Autophosphorylated1
  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus
  • Selected DME Specific Peptides for CDKL5 (O76039) (see all 6)
     WSVGCIL  SEIDQLF  KLYLVFE  PYGKSVD 


    See CDKL5 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins (2 alternative transcripts): 
    NP_001032420.1  NP_003150.1  

    ENSEMBL proteins: 
     ENSP00000369332   ENSP00000369325  

    CDKL5 Human Recombinant Protein Products:

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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    HGNC Gene Families:
    CDK: Cyclin-dependent kinases

    IUPHAR Guide to PHARMACOLOGY protein family classification: cyclin-dependent kinase-like 5
    Cyclin-dependent kinase-like (CDKL) family

    5 InterPro protein domains:
     IPR017441 Protein_kinase_ATP_BS
     IPR002290 Ser/Thr_dual-sp_kinase_dom
     IPR011009 Kinase-like_dom
     IPR008271 Ser/Thr_kinase_AS
     IPR000719 Prot_kinase_dom

    Graphical View of Domain Structure for InterPro Entry O76039

    ProtoNet protein and cluster: O76039

    UniProtKB/Swiss-Prot: CDKL5_HUMAN, O76039
    Similarity: Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. CDC2/CDKX subfamily
    Similarity: Contains 1 protein kinase domain


    Find genes that share domains with CDKL5           About GenesLikeMe


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: CDKL5_HUMAN, O76039
    Function: Mediates phosphorylation of MECP2
    Catalytic activity: ATP + a protein = ADP + a phosphoprotein

         Enzyme Numbers (IUBMB): EC 2.7.11.221 2 EC 2.7.112

         Gene Ontology (GO): Selected molecular function terms (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004672protein kinase activity IDA16935860
    GO:0004674protein serine/threonine kinase activity TAS9721213
    GO:0004693cyclin-dependent protein serine/threonine kinase activity IEA--
    GO:0004713protein tyrosine kinase activity ----
    GO:0005524ATP binding IDA16935860
         
    Find genes that share ontologies with CDKL5           About GenesLikeMe


    Phenotypes:
         4 GenomeRNAi human phenotypes for CDKL5:
     Decreased focal adhesion (FA)   Decreased substrate adherent c  Increased cell death in HCC-19  Increased colony dispersion (i 

         3 MGI mutant phenotypes (inferred from 1 allele(MGI details for Cdkl5):
     behavior/neurological  nervous system  taste/olfaction 

    Find genes that share phenotypes with CDKL5           About GenesLikeMe

    Animal Models:
         MGI mouse knock-out Cdkl5tm1.1Joez for CDKL5

       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for CDKL5
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    miRTarBase miRNAs that target CDKL5:
    hsa-mir-222-3p (MIRT046657)

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    Sino Biological Human cDNA Clone for CDKL5
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CDKL5


    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from UniProtKB/Swiss-Prot
    CDKL5_HUMAN, O76039: Nucleus
    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    nucleus5
    cytosol2

    Gene Ontology (GO): Selected cellular component terms (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm IDA--
    GO:0032587colocalizes with ruffle membrane ISS--
    GO:0032839dendrite cytoplasm ISS--

    Find genes that share ontologies with CDKL5           About GenesLikeMe


    (SuperPaths according to PathCards, Pathways according to R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to QIAGEN, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene).
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    SuperPaths for CDKL5 About    
    See pathways by source

    SuperPathContained pathways About
    1Sweet Taste Signaling
    Sperm Motility0.37
    2BDNF signaling pathway
    BDNF signaling pathway

    1 Downloadable PowerPoint Slide of GeneGlobe Pathway Central Maps for CDKL5
        Sperm Motility

    1 BioSystems Pathway for CDKL5
        BDNF signaling pathway



        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for CDKL5
    Interactions:

        Search GeneGlobe Interaction Network for CDKL5

    STRING Interaction Network Preview (showing 5 interactants - click image to see 6)

    Selected Interacting proteins for CDKL5 (O760392, 3 ENSP000003693254) via UniProtKB, MINT, STRING, and/or I2D (see all 8)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    ABL1P005192, 3, ENSP000003614234MINT-8110107 I2D: score=3 STRING: ENSP00000361423
    FYNP062412, 3, ENSP000003576564MINT-8111019 I2D: score=3 STRING: ENSP00000357656
    MECP2P516083, ENSP000003955354I2D: score=1 STRING: ENSP00000395535
    GRB2P629933, ENSP000003390074I2D: score=2 STRING: ENSP00000339007
    MGMTENSP000003021114STRING: ENSP00000302111
    About this table

    Gene Ontology (GO): Selected biological process terms (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001764neuron migration ISS--
    GO:0006468protein phosphorylation TAS9721213
    GO:0032855positive regulation of Rac GTPase activity ISS--
    GO:0045773positive regulation of axon extension ISS--
    GO:0046777protein autophosphorylation IDA16935860

    Find genes that share ontologies with CDKL5           About GenesLikeMe



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for CDKL5

    2 HMDB Compounds for CDKL5    About this table
    CompoundSynonyms CAS #PubMed Ids
    ADPadenosindiphosphorsaeure (see all 8)58-64-0--
    Adenosine triphosphate5'-(tetrahydrogen triphosphate) Adenosine (see all 24)56-65-5--



    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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    REFSEQ mRNAs for CDKL5 gene (2 alternative transcripts): 
    NM_001037343.1  NM_003159.2  

    Unigene Cluster for CDKL5:

    Cyclin-dependent kinase-like 5
    Hs.659851  [show with all ESTs]
    Unigene Representative Sequence: BC036091
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000379996(uc022btn.1 uc004cym.3) ENST00000379989(uc004cyn.3)
    ENST00000463994
    miRNA
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      QuantiFast Probe-based Assays in human, mouse, rat CDKL5

    Additional mRNA sequence: 

    AK056879.1 AK307444.1 AY217744.1 BC010966.1 BC036091.1 HQ171445.1 X89059.1 Y15057.1 

    4 DOTS entries:

    DT.409032  DT.97771331  DT.95234867  DT.75136827 

    22 AceView cDNA sequences:

    NM_003159 AA398911 AY217744 BC010966 Y15057 AI569744 CD675032 AK056879 
    W07775 AI582736 BI559845 CB153498 BX096833 BE831003 BC036091 X89059 
    AL704691 AA403214 AI286150 N80713 BF679133 AA228740 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for CDKL5    About this scheme

    ExUns: 1 ^ 2a · 2b · 2c ^ 3 ^ 4 ^ 5a · 5b ^ 6 ^ 7 ^ 8a · 8b ^ 9a · 9b ^ 10 ^ 11 ^ 12 ^ 13
    SP1:                                -                                                                           
    SP2:        -     -     -     -     -                                                                           
    SP3:                                -                                                                           
    SP4:                                                                                                            
    SP5:                                                                                                            


    ECgene alternative splicing isoforms for CDKL5

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    CDKL5 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GAAGAACCAA
    CDKL5 Expression
    About this image


    CDKL5 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 4) fully expand
     
     Brain (Nervous System)    fully expand to see all 2 entries
             Cerebral Cortex
     
     Trophoblast (Extraembryonic Tissues)
             Trophoblast Cells Trophoblast
     
     Testis (Reproductive System)
             Leydig Cells Testis Interstitium
     
     Bone (Muscoskeletal System)
             Bone Marrow
    CDKL5 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    CDKL5 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.659851

    UniProtKB/Swiss-Prot: CDKL5_HUMAN, O76039
    Tissue specificity: Expressed in brain, lung, kidney, prostate, ovary, placenta, pancreas and testis

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CDKL5

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
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    This gene was present in the common ancestor of animals and fungi.

    Orthologs for CDKL5 gene from Selected species (see all 16)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cdkl51 , 5 cyclin-dependent kinase-like 51, 5 89.38(n)1
    95.8(a)1
      X (73.95 cM)5
    3822531  NM_001024624.21  NP_001019795.11 
     1607843085 
    chicken
    (Gallus gallus)
    Aves CDKL51 cyclin-dependent kinase-like 5 79.68(n)
    83.54(a)
      428001  XM_425571.3  XP_425571.2 
    lizard
    (Anolis carolinensis)
    Reptilia CDKL56
    cyclin-dependent kinase-like 5
    75(a)
    1 ↔ 1
    3(122890920-123000894)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.228262 Xenopus laevis transcribed sequence with strong similarity more 84.46(n)    BJ059534.1 
    zebrafish
    (Danio rerio)
    Actinopterygii cdkl51 cyclin-dependent kinase-like 5 65.86(n)
    68.02(a)
      559341  NM_001130771.1  NP_001124243.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG68006
    --
    32(a)
    1 → many
    3R(17601860-17602935)
    worm
    (Caenorhabditis elegans)
    Secernentea dyf-186
    Protein DYF-18 (dyf-18) mRNA, complete cds
    31(a)
    1 → many
    IV(11798665-11801088) WBGene00010349
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes KIN286
    Serine/threonine protein kinase, subunit of the tr...
    31(a)
    1 → many
    IV(267698-268699) YDL108W


    ENSEMBL Gene Tree for CDKL5 (if available)
    TreeFam Gene Tree for CDKL5 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for CDKL5 gene
    CDKL12  CDK202  CDKL22  CDKL32  CDK72  CDKL42  
    17 SIMAP similar genes for CDKL5 using alignment to 1 protein entry:     CDKL5_HUMAN:
    CDK2    CDK3    CDK7    CDKL2    PCTK1    MAPK1
    CDK6    CDK4    CDK10    GSK3B    MAPK12    MAPK14
    MAPK11    MAPK13    CDK9    MAPK8    MOK

    Find genes that share paralogs with CDKL5           About GenesLikeMe



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for CDKL5 (see all 2742)    About this table                                 

    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    VAR_0580284
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0580282 T I mis40--------
    VAR_0580254
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0580252 H R mis40--------
    VAR_0580224
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0580222 A V mis40--------
    VAR_0580304
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0580302 N T mis40--------
    VAR_0376354
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0376352 P L mis40--------
    VAR_0419984
    An ovarian serous carcinoma sample4--see VAR_0419982 P Q mis40--------
    VAR_0419974
    A metastatic melanoma sample4--see VAR_0419972 A T mis40--------
    VAR_0365784
    A colorectal cancer sample4--see VAR_0365782 N H mis40--------
    VAR_0580294
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0580292 C Y mis40--------
    VAR_0235614
    Epileptic encephalopathy, early infantile, 2 (EIEE2)4--see VAR_0235612 R S mis40--------

    HapMap Linkage Disequilibrium report for CDKL5 (18443703 - 18671749 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for CDKL5:    About this table    
    Variant IDTypeSubtypePubMed ID
    nsv6821CNV Insertion18451855
    nsv528654CNV Gain19592680

    Human Gene Mutation Database (HGMD): CDKL5
    Locus Specific Mutation Databases (LSDB): CDKL5

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing CDKL5
    DNA2.0 Custom Variant and Variant Library Synthesis for CDKL5

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

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    OMIM gene information: 300203   
    OMIM disorders: 300672  105830  
    UniProtKB/Swiss-Prot: CDKL5_HUMAN, O76039
  • Note=Chromosomal aberrations involving CDKL5 are found in patients manifesting early-onset seizures and
    spams and psychomotor impairment. Translocation t(X;6)(p22.3;q14); translocation t(X;7)(p22.3;p15)
  • Epileptic encephalopathy, early infantile, 2 (EIEE2) [MIM:300672]: A severe form of epilepsy
    characterized by seizures or spasms beginning in infancy. Patients with epileptic encephalopathy early infantile
    type 2 manifest features resembling Rett syndrome such as microcephaly, lack of speech development, stereotypic
    hand movements. However, EIEE2 and Rett syndrome are considered two distinct entities. Note=The disease is caused
    by mutations affecting the gene represented in this entry

  • 12 diseases for CDKL5:    
    About MalaCards
    epileptic encephalopathy, early infantile, 2    cdkl5-related angelman-like syndrome    west syndrome    angelman syndrome-like
    atypical rett syndrome    gait apraxia    epileptic encephalopathy, early infantile, 5    seizure disorder
    rett syndrome    epileptic encephalopathy, early infantile, 17    aicardi syndrome    angelman syndrome

    6 diseases from the University of Copenhagen DISEASES database for CDKL5:
    Rett syndrome     Intellectual disability     Aicardi syndrome     Microcephaly
    Gait apraxia     Brain disease

    Find genes that share disorders with CDKL5           About GenesLikeMe

    8 Novoseek inferred disease relationships for CDKL5 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    rett syndrome 94.3 46 19740913 (2), 18701457 (2), 16813600 (2), 19241098 (2) (see all 26)
    infantile spasms 91.6 43 16806828 (2), 15689447 (2), 17049193 (2), 16935860 (2) (see all 21)
    cryptogenic west syndrome 85.5 1 16806828 (1)
    severe mental retardation 68.7 3 20513142 (1), 12736870 (1), 16015284 (1)
    mental retardation 68.5 12 16935860 (2), 15492925 (2), 20397747 (1), 15499549 (1) (see all 7)
    encephalopathy 67.7 19 17256798 (2), 17993579 (2), 19780792 (2), 19740913 (1) (see all 11)
    epilepsy 65.3 34 18266744 (5), 19780792 (3), 19428276 (2), 16326141 (2) (see all 14)
    myoclonic seizure 63.2 2 16326141 (1), 17049193 (1)

    Genetic Association Database (GAD): CDKL5
    Human Genome Epidemiology (HuGE) Navigator: CDKL5 (11 documents)

    Export disorders for CDKL5 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

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    PubMed articles for CDKL5 gene, integrated from 10 sources (see all 85) (see top 10):
    (articles sorted by number of sources associating them with CDKL5)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation. (PubMed id 16935860)1, 2, 3, 9 Bertani I.... Kilstrup-Nielsen C. (J. Biol. Chem. 2006)
    2. CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients. (PubMed id 16611748)1, 2, 4 Archer H.L.... Osborne J. (J. Med. Genet. 2006)
    3. Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region. (PubMed id 9721213)1, 2, 3 Montini E.... Franco B. (Genomics 1998)
    4. Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy. (PubMed id 19780792)1, 4, 9 Mei D....Guerrini R. (Epilepsia 2010)
    5. CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome. (PubMed id 15917271)1, 2, 9 Mari F.... Landsberger N. (Hum. Mol. Genet. 2005)
    6. Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature. (PubMed id 19793311)1, 4, 9 Nemos C....Philippe C. (Clin. Genet. 2009)
    7. Key clinical features to identify girls with CDKL5 mutations. (PubMed id 18790821)1, 2, 9 Bahi-Buisson N.... Bienvenu T. (Brain 2008)
    8. Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy. (PubMed id 17993579)1, 2, 9 Rosas-Vargas H.... Bienvenu T. (J. Med. Genet. 2008)
    9. [Methyl-CpG-binding protein 2 gene and CDKL5 gene mutation in patients with Rett syndrome: analysis of 177 Chinese pediatric patients]. (PubMed id 19552836)1, 4, 9 Li M.R....Wu X.R. (Zhonghua Yi Xue Za Zhi 2009)
    10. Early onset seizures and Rett-like features associated with mutations in CDKL5. (PubMed id 16015284)1, 2, 9 Evans J.C.... Clarke A.J. (Eur. J. Hum. Genet. 2005)
    11. Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. (PubMed id 15492925)1, 2, 9 Weaving L.S.... Gecz J. (Am. J. Hum. Genet. 2004)
    12. Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes. (PubMed id 19241098)1, 2, 9 Russo S.... Larizza L. (Neurogenetics 2009)
    13. MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome. (PubMed id 17089071)1, 4, 9 Li M.R....Wu X.R. (J. Hum. Genet. 2007)
    14. CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms. (PubMed id 15689447)1, 2, 9 Scala E....Renieri A. (J. Med. Genet. 2005)
    15. Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation. (PubMed id 15499549)1, 2, 9 Tao J.... Kalscheuer V.M. (Am. J. Hum. Genet. 2004)
    16. Disruption of the serine/threonine kinase 9 gene causes severe X- linked infantile spasms and mental retardation. (PubMed id 12736870)1, 2, 9 Kalscheuer V.M.... Gecz J. (Am. J. Hum. Genet. 2003)
    17. Epilepsy in Rett syndrome: clinical and genetic features. (PubMed id 20728410)1, 4 Pintaudi M....Veneselli E. (amp 2010)
    18. CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy. (PubMed id 18809835)1, 2 Elia M.... Fichera M. (Neurology 2008)
    19. The DNA sequence of the human X chromosome. (PubMed id 15772651)1, 2 Ross M.T.... Bentley D.R. (Nature 2005)
    20. Differential screening leads to novel genetic markers of monocyte to macrophage maturation. (PubMed id 8864140)1, 2 Krause S.W....Andreesen J.D. (J. Leukoc. Biol. 1996)
    21. CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery. (PubMed id 19740913)1, 9 Ricciardi S....Broccoli V. (Hum. Mol. Genet. 2009)
    22. A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. (PubMed id 19253388)2, 9 Sprovieri T.... Quattrone A. (Am. J. Med. Genet. A 2009)
    23. CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail. (PubMed id 18701457)1, 9 Rusconi L....Landsberger N. (J. Biol. Chem. 2008)
    24. The three stages of epilepsy in patients with CDKL5 mutations. (PubMed id 18266744)1, 9 Bahi-Buisson N....Bienvenu T. (Epilepsia 2008)
    25. Seizures and electroencephalographic findings in CDKL5 mutations: case report and review. (PubMed id 17049193)1, 9 Grosso S....Balestri P. (amp 2007)
    26. A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder. (PubMed id 19428276)1, 9 Psoni S....Kitsiou-Tzeli S. (Eur. J. Paediatr. Neurol. 2010)
    27. Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders. (PubMed id 20397747)1, 9 White R....Christodoulou J. (Twin Res Hum Genet 2010)
    28. Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder. (PubMed id 19471977)1, 9 Erez A....Lalani S.R. (Neurogenetics 2009)
    29. Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature. (PubMed id 18063413)1, 9 Pintaudi M....Veneselli E. (amp 2008)
    30. Myoclonic encephalopathy in the CDKL5 gene mutation. (PubMed id 16326141)1, 9 Buoni S....Hayek J. (Clin Neurophysiol 2006)
    31. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. (PubMed id 20513142)1, 9 Zweier M....Rauch A. (Hum. Mutat. 2010)
    32. Validation of high-resolution DNA melting analysis for mutation scanning of the CDKL5 gene: identification of novel mutations. (PubMed id 23064044)1 Raymond L....Bienvenu T. (Gene 2013)
    33. Epileptic encephalopathy and atypical Rett syndrome with mutations in CDKL5: clinical and molecular characterization of two Brazilian patients. (PubMed id 23828526)1 Ermel E.L....Raskin S. (Arq Neuropsiquiatr 2013)
    34. CDKL5 mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 patients. (PubMed id 22832775)1 JAohn J....Muhle H. (J. Child Neurol. 2013)
    35. The protein interaction landscape of the human CMGC kinase group. (PubMed id 23602568)1 Varjosalo M....Gstaiger M. (Cell Rep 2013)
    36. Novel mutations in cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndrome. (PubMed id 23242510)1 Das D.K....Udani V. (Neuromolecular Med. 2013)
    37. CDKL5 and ARX mutations in males with early-onset epilepsy. (PubMed id 23583054)1 Mirzaa G.M....Das S. (Pediatr. Neurol. 2013)
    38. Respiratory and sleep disorders in female children with atypical Rett syndrome caused by mutations in the CDKL5 gene. (PubMed id 23151060)1 Hagebeuk E.E....de Weerd A.W. (Dev Med Child Neurol 2013)
    39. Historic, clinical, and prognostic features of epileptic encephalopathies caused by CDKL5 mutations. (PubMed id 22264704)1 Moseley B.D....Nickels K.C. (Pediatr. Neurol. 2012)
    40. Variant of Rett syndrome and CDKL5 gene: clinical and autonomic description of 10 cases. (PubMed id 22430159)1 Pini G....Zappella M. (Neuropediatrics 2012)
    41. CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons. (PubMed id 22922712)1 Ricciardi S....Broccoli V. (Nat. Cell Biol. 2012)
    42. Clinical phenotype of 5 females with a CDKL5 mutation. (PubMed id 21765152)1 Stalpers X.L....Verrips A. (J. Child Neurol. 2012)
    43. CDKL5, a novel MYCN-repressed gene, blocks cell cycle and promotes differentiation of neuronal cells. (PubMed id 22921766)1 Valli E....Ciani E. (Biochim. Biophys. Acta 2012)
    44. CDKL5 gene status in female patients with epilepsy and Rett-like features: two new mutations in the catalytic domain. (PubMed id 22867051)1 Maortua H....Tejada M.I. (BMC Med. Genet. 2012)
    45. Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships. (PubMed id 22678952)1 Bahi-Buisson N....Bienvenu T. (Am. J. Med. Genet. A 2012)
    46. A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain. (PubMed id 21748340)2 Williamson S.L.... Christodoulou J. (Hum. Genet. 2012)
    47. What we know and would like to know about CDKL5 and its involvement in epileptic encephalopathy. (PubMed id 22779007)1 Kilstrup-Nielsen C....Landsberger N. (Neural Plast. 2012)
    48. A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence. (PubMed id 21502606)1 Klein K.M....Scheffer I.E. (Neurology 2011)
    49. An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brain. (PubMed id 21124335)1 Fichou Y....Bienvenu T. (J. Hum. Genet. 2011)
    50. Toward an understanding of the protein interaction network of the human liver. (PubMed id 21988832)1 Wang J....Yang X. (Mol. Syst. Biol. 2011)
    51. Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathy. (PubMed id 21107515)1 Nectoux J....Bienvenu T. (J. Mol. Med. 2011)
    52. Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features. (PubMed id 21318334)1 Rademacher N....Kalscheuer V.M. (Neurogenetics 2011)
    53. Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity. (PubMed id 21775177)1 Intusoma U....Limprasert P. (Eur. J. Paediatr. Neurol. 2011)
    54. Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females. (PubMed id 21293276)1 Bartnik M....Stankiewicz P. (Genet. Med. 2011)
    55. CDKL5 alterations lead to early epileptic encephalopathy in both genders. (PubMed id 21770923)1 Liang J.S....Yamamoto T. (Epilepsia 2011)
    56. Epilepsy caused by CDKL5 mutations. (PubMed id 20493745)1 CastrAcn M....Ala-Mello S. (Eur. J. Paediatr. Neurol. 2011)
    57. iPS cells to model CDKL5-related disorders. (PubMed id 21750574)1 Amenduni M....Meloni I. (Eur. J. Hum. Genet. 2011)
    58. CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life. (PubMed id 21309761)1 Melani F....Guerrini R. (Dev Med Child Neurol 2011)
    59. The SH3 domain of postsynaptic density 95 mediates inflammatory pain through phosphatidylinositol-3-kinase recruitment. (PubMed id 20467438)1 Arbuckle M.I....Grant S.G. (EMBO Rep. 2010)
    60. Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in males. (PubMed id 20602487)1 Masliah-Plachon J....Bienvenu T. (Am. J. Med. Genet. A 2010)
    61. Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis. (PubMed id 20068231)2 Olsen J.V....Mann M. (Sci. Signal. 2010)
    62. CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy. (PubMed id 19734009)1 Nabbout R....Bahi-Buisson N. (Epilepsy Res. 2009)
    63. Large-scale proteomics analysis of the human kinome. (PubMed id 19369195)2 Oppermann F.S.... Daub H. (Mol. Cell. Proteomics 2009)
    64. Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy. (PubMed id 19564592)1 Fichou Y....Bienvenu T. (Neurology 2009)
    65. Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle. (PubMed id 18691976)2 Daub H.... Mann M. (Mol. Cell 2008)
    66. A quantitative atlas of mitotic phosphorylation. (PubMed id 18669648)2 Dephoure N.... Gygi S.P. (Proc. Natl. Acad. Sci. U.S.A. 2008)
    67. Toward a confocal subcellular atlas of the human proteome. (PubMed id 18029348)1 Barbe L....Andersson-Svahn H. (amp 2008)
    68. Patterns of somatic mutation in human cancer genomes. (PubMed id 17344846)2 Greenman C.... Stratton M.R. (Nature 2007)
    69. Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening. (PubMed id 17474147)1 Wu C....Li S.S. (Proteomics 2007)
    70. The consensus coding sequences of human breast and colorectal cancers. (PubMed id 16959974)2 Sjoeblom T.... Velculescu V.E. (Science 2006)
    71. Rett syndrome: clinical review and genetic update. (PubMed id 15635068)1 Weaving L.S....Christodoulou J. (J. Med. Genet. 2005)
    72. Proteomic analysis of human O6-methylguanine-DNA methyltransferase by affinity chromatography and tandem mass spectrometry. (PubMed id 16226712)1 Niture S.K....Srivenugopal K.S. (Biochem. Biophys. Res. Commun. 2005)
    73. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1 Gerhard D.S.... Malek J. (Genome Res. 2004)
    74. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (Proc. Natl. Acad. Sci. U.S.A. 2002)
    75. Angelman Syndrome (PubMed id 20301323)1 Pagon R.A....Stephens K. (1993)
    76. CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disorders. (PubMed id 16330482)9 Lin C....Rosner M.R. (Hum. Mol. Genet. 2005)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 6792 HGNC: 11411 AceView: CDKL5 Ensembl:ENSG00000008086 euGenes: HUgn6792
    ECgene: CDKL5 H-InvDB: CDKL5

    (According to HUGE)
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      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
    About This Section

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    NameDescription
    PharmGKB entry for CDKL5 Pharmacogenomics, SNPs, Pathways
    GeneReviewshttp://www.ncbi.nlm.nih.gov/books/NBK1116/?term=CDKL5[genesymbol]

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    Patent Information for CDKL5 gene:
    Search GeneIP for patents involving CDKL5

    GeneCards and IP:
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