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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

CPLX1 Gene

protein-coding   GIFtS: 59
GCID: GC04M000778

complexin 1
 Explore 5 diseases affiliated with
CPLX1 via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for CPLX1    

Aliases
for CPLX1 gene

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section
Aliases
Complexin 11 2     Complexin-11
CPX-I1 2     Synaphin 22
Complexin I2 3     Synaphin-23
CPX I2 3     Synaphin-23
CPX12 5     

External Ids:    HGNC: 23091   Entrez Gene: 108152   Ensembl: ENSG000001689937   OMIM: 6050325   UniProtKB: O148103   

Export aliases for CPLX1 gene to outside databases

Previous GC identifers: GC04M000804 GC04M000769 GC04M000770 GC04M000771 GC04M000749


Summaries
for CPLX1 gene

(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section
Entrez Gene summary for CPLX1:
Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle
exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the
SNAP receptor complex and disrupts it, allowing transmitter release. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: CPLX1_HUMAN, O14810
Function: Positively regulates a late step in synaptic vesicle exocytosis. Organizes the SNAREs into a cross-linked
zigzag topology that, when interposed between the vesicle and plasma membranes, is incompatible with fusion, thereby
preventing SNAREs from releasing neurotransmitters until an action potential arrives at the synapse. Also involved in
glucose-induced secretion of insulin by pancreatic beta-cells (By similarity)

Gene Wiki entry for CPLX1


Genomic Views
for CPLX1 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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000004.11  NC_018915.1  NT_037622.5  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the CPLX1 gene promoter:
         Sp1   HTF   Egr-4   CREB   deltaCREB   Cart-1   Msx-1   Pax-4a   LyF-1   ATF6   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for CPLX1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat CPLX1


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

Entrez Gene cytogenetic band: 4p16.3   Ensembl cytogenetic band:  4p16.3   HGNC cytogenetic band: 4p16.3

CPLX1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
CPLX1 gene location

GeneLoc information about chromosome 4         GeneLoc Exon Structure

GeneLoc location for GC04M000778:  view genomic region     (about GC identifiers)

Start:
 778,745 bp from pter      End:
 819,986 bp from pter
Size:
 41,242 bases      Orientation:
 minus strand

Proteins
for CPLX1 gene

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, 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, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section
UniProtKB/Swiss-Prot: CPLX1_HUMAN, O14810 (See protein sequence)
Recommended Name: Complexin-1  
Size: 134 amino acids; 15030 Da
Subunit: Binds to the SNARE core complex containing SNAP25, VAMP2 and STX1A
Subcellular location: Cytoplasm, cytosol (By similarity). Note=Enriched at synaptic-releasing sites in mature neurons
(By similarity)
2 PDB 3D structures from and Proteopedia for CPLX1:
3RK3 (3D)        3RL0 (3D)    
Secondary accessions: A6NI80 B2R4R5 D3DVN3

Explore the universe of human proteins at neXtProt for CPLX1: NX_O14810

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O14810

    • CPLX1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_006642.1  
    ENSEMBL proteins: 
     ENSP00000305613   ENSP00000425960   ENSP00000421947   ENSP00000426156  
    Reactome Protein details: O14810
    Human Recombinant Protein Products: 
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    Uscn Proteins for CPLX1

    Gene Ontology (GO): 5/7 cellular component terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005829cytosol TAS--
    GO:0030425dendrite IEA--
    GO:0031201SNARE complex ----
    GO:0043025neuronal cell body IEA--
    GO:0043234protein complex ----


    CPLX1 for ontologies           About GeneDecksing



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    Protein Domains /
    Families
    for CPLX1 gene

    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    CPLX1 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR008849 Synaphin

    Graphical View of Domain Structure for InterPro Entry O14810

    ProtoNet protein and cluster: O14810

    1 Blocks protein family: IPB008849 Synaphin

    UniProtKB/Swiss-Prot: CPLX1_HUMAN, O14810
    Similarity: Belongs to the complexin/synaphin family


    Function
    for CPLX1 gene

    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section
    Function Summary:

         UniProtKB/Swiss-Prot: CPLX1_HUMAN, O14810
    Function: Positively regulates a late step in synaptic vesicle exocytosis. Organizes the SNAREs into a cross-linked
    zigzag topology that, when interposed between the vesicle and plasma membranes, is incompatible with fusion, thereby
    preventing SNAREs from releasing neurotransmitters until an action potential arrives at the synapse. Also involved in
    glucose-induced secretion of insulin by pancreatic beta-cells (By similarity)

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    hsa-miR-185* hsa-miR-99b* hsa-miR-4272 hsa-miR-765 hsa-miR-25 hsa-miR-570 hsa-miR-421 hsa-miR-34b
    SwitchGear 3'UTR luciferase reporter plasmid: CPLX1 3' UTR sequence
    Inhib. RNA
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    Gene Editing
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    Clone
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    In Situ Assay
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    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000149SNARE binding ----
    GO:0005326neurotransmitter transporter activity IEA--
    GO:0017075syntaxin-1 binding IEA--
    GO:0019905syntaxin binding ----


    CPLX1 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for CPLX1:
     Decreased influenza A virus in 

    Animal Models:
         Mouse knock-out Cplx1tm1Rmnd for CPLX1
         6 MGI mutant phenotypes (inferred from 1 allele) (MGI details for Cplx1):
     behavior/neurological  growth/size  hearing/vestibular/ear  mortality/aging  nervous system 
     reproductive system 

    CPLX1 for phenotypes           About GeneDecksing


    Pathways & Interactions
    for CPLX1 gene

    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, 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 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Serotonin Neurotransmitter Release Cycle
    		Serotonin Neurotransmitter Release Cycle1.00
    		Acetylcholine Neurotransmitter Release Cycle0.53
    		Dopamine Neurotransmitter Release Cycle1.00
    		Glutamate Neurotransmitter Release Cycle0.42
    		Norepinephrine Neurotransmitter Release Cycle0.60
    2GABA synthesis, release, reuptake and degradation
    		GABA synthesis, release, reuptake and degradation1.00
    		Neurotransmitter Release Cycle0.53
    3Transmission across Chemical Synapses
    		Transmission across Chemical Synapses1.00
    		Neuronal System0.67
    4Synaptic Vesicle Pathway
    		Synaptic Vesicle Pathway1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    1 BioSystems Pathway for CPLX1 
        Synaptic Vesicle Pathway

    5/9        Reactome Pathways for CPLX1 (see all 9)
        Acetylcholine Neurotransmitter Release Cycle
    Transmission across Chemical Synapses
    GABA synthesis, release, reuptake and degradation
    Neurotransmitter Release Cycle
    Neuronal System



    CPLX1 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for CPLX1

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/33 Interacting proteins for CPLX1 (O148103 ENSP000003056134) via UniProtKB, MINT, STRING, and/or I2D (see all 33)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    VAMP2P630273, ENSP000003142144I2D: score=3 STRING: ENSP00000314214
    STX1AQ166233, ENSP000002228124I2D: score=3 STRING: ENSP00000222812
    SNAP25P608803, ENSP000002549764I2D: score=1 STRING: ENSP00000254976
    RXRBP287023I2D: score=1 
    DNAJC5ENSP000003541114STRING: ENSP00000354111
    About this table

    Gene Ontology (GO): 5/7 biological process terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006836neurotransmitter transport ----
    GO:0006887exocytosis TAS7553862
    GO:0007268synaptic transmission TAS--
    GO:0007269neurotransmitter secretion TAS--
    GO:0014047glutamate secretion TAS--


    CPLX1 for ontologies           About GeneDecksing



    Drugs & Compounds
    for CPLX1 gene

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for CPLX1
    Search CenterWatch for drugs/clinical trials and news about CPLX1 

    Transcripts
    for CPLX1 gene

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 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,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section
    REFSEQ mRNAs for CPLX1 gene: 
    NM_006651.3  

    Unigene Cluster for CPLX1:

    Complexin 1
    Hs.478930  [show with all ESTs]
    Unigene Representative Sequence: NM_006651
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000304062(uc003gbi.3 uc003gbj.3) ENST00000505203 ENST00000506404
    ENST00000504062 ENST00000513195

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    hsa-miR-185* hsa-miR-99b* hsa-miR-4272 hsa-miR-765 hsa-miR-25 hsa-miR-570 hsa-miR-421 hsa-miR-34b
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    Inhib. RNA
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    Additional cDNA sequence: 

    AB593095.1 AF022383.1 AK126578.1 AK311921.1 BC002471.2 BT007029.1 

    6 DOTS entries:

    DT.408291  DT.101980599  DT.100036075  DT.92065654  DT.40120035  DT.92422340 

    24/80 AceView cDNA sequences (see all 80):

    T34916 AA323455 BM543581 CR603035 BI489595 BU739726 BQ130485 AI886623 
    BE222735 NM_006651 CK300528 BM714837 BT007029 BM716718 AK126578 AW296025 
    CB153682 BU728350 BX425363 BU187125 AI207968 AF022383 BX446900 BQ189473 

    GeneLoc Exon Structure

    4 Alternative Splicing Database (ASD) splice patterns (SP) for CPLX1    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3 ^ 4a · 4b ^ 5a · 5b · 5c
    SP1:                    -     -                           
    SP2:                    -     -                           
    SP3:                          -                           
    SP4:                                                      


    ECgene alternative splicing isoforms for CPLX1

    Expression
    for CPLX1 gene

    (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™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    CPLX1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TCGGGGCCCC

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)
    About this image

    CPLX1 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    8 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    OvaryPrimary FollicleGranulosa CellsOvary
    Spinal CordSpinal Ventral ColumnsVentral Spinal Cord Progenitor CellsMotor Neurons
    BrainCerebral CortexBrain
    BrainMedulla OblongataBrain
    BrainMidbrain tegmentumBrain
    EyeRetinaEye
    Neural TubeMetencephalonNeural Tube
    Spinal CordSpinal Ventral ColumnsSpinal Cord
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See CPLX1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for CPLX1

    SOURCE GeneReport for Unigene cluster: Hs.478930

    UniProtKB/Swiss-Prot: CPLX1_HUMAN, O14810
    Tissue specificity: Nervous system. In hippocampus and cerebellum, expressed mainly by inhibitory neurons.
    Overexpressed in substantia nigra from patients with Parkinson disease

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    In Situ
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    Orthologs
    for CPLX1 gene

    (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)
    About This Section
    This gene was present in the common ancestor of animals.

    Orthologs for CPLX1 gene from 5/14 species (see all 14)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    chicken
    (Gallus gallus)    		 Aves CPLX21 complexin 2 79.85(n)
    91.79(a)    		   427286  XM_424869.3  XP_424869.1 
    lizard
    (Anolis carolinensis)    		 Reptilia CPLX16
    		 --
    		 93(a)
    		 1 ↔ 1
    		 GL343201.1(1682864-1908184)
    zebrafish
    (Danio rerio)    		 Actinopterygii wufc97e102 Transcribed sequence with moderate similarity to protein more 74.67(n)    CK363405.1 
    fruit fly
    (Drosophila melanogaster)    		 Insecta cpx6
    		 complexin
    		 37(a)
    		 1 → many
    		 3R(105906-130349)
    worm
    (Caenorhabditis elegans)    		 Secernentea cpx-16
    		 Putative complexin-1
    		 34(a)
    		 1 → many
    		 I(1594658-1596177)


    ENSEMBL Gene Tree for CPLX1 (if available)
    TreeFam Gene Tree for CPLX1 (if available) 

    Paralogs
    for CPLX1 gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for CPLX1 gene
    CPLX22  
    1 SIMAP similar gene for CPLX1 using alignment to 5 protein entries:     CPLX1_HUMAN (see all proteins):
    CPLX2

    CPLX1 for paralogs           About GeneDecksing



    Genomic Variants
    for CPLX1 gene

    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, 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) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 6 variations for CPLX1
         6 CNVs: 32564 9466 3475 30188 7453 51459
    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing CPLX1
    DNA2.0 Custom Variant and Variant Library Synthesis for CPLX1

    Disorders / Diseases
    for CPLX1 gene

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    CPLX1 for disorders           About GeneDecksing

    OMIM gene information: 605032    OMIM disorders: --

    5 diseases for CPLX1:    About MalaCards
    wernicke encephalopathy    parkinson's disease    schizophrenia    pancreatitis
    neuronitis

    2 diseases from the University of Copenhagen DISEASES database for CPLX1:
    Wernicke encephalopathy     Schizophrenia
    Human Genome Epidemiology (HuGE) Navigator: CPLX1 (2 documents)

    Export disorders for CPLX1 gene to outside databases

    Publications
    for CPLX1 gene

    (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

    PubMed articles for CPLX1 gene, integrated from 9 sources (see all 30):
    (articles sorted by number of sources associating them with CPLX1)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Complexins: cytosolic proteins that regulate SNAP receptor function. (PubMed id 7553862)1, 2, 3 McMahon H.T.... Suedhof T.C. (1995)
    2. Complexin cross-links prefusion SNAREs into a zigzag array. (PubMed id 21785414)1, 2 Kummel D.... Reinisch K.M. (2011)
    3. Proteome analysis of human substantia nigra in Parkinson's disease. (PubMed id 15526345)1, 2 Basso M....Fasano M. (2004)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    5. Cerebellar synaptic protein expression in schizophrenia. (PubMed id 11483314)1, 2 Eastwood S.L.... Harrison P.J. (2001)
    6. Preferential involvement of excitatory neurons in medial temporal lobe in schizophrenia. (PubMed id 9853440)1, 2 Harrison P.J. and Eastwood S.L. (1998)
    7. Regulation of complexin 1 and complexin 2 in the developing human prefrontal cortex. (PubMed id 18240322)1, 9 Salimi K....Jarskog L.F. (2008)
    8. No association of complexin1 and complexin2 genes with schizophrenia in a Japanese population. (PubMed id 16442780)1, 9 Kishi T....Iwata N. (2006)
    9. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    10. Complexin arrests a pool of docked vesicles for fast C a2+-dependent release. (PubMed id 22705946)1 Malsam J....Sollner T.H. (2012)

    External Searches for CPLX1 gene

    (in PubMed, OMIM, and NCBI Bookshelf)
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    Genome Databases showing CPLX1 gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 10815 HGNC: 2309 AceView: CPLX1 Ensembl:ENSG00000168993 euGenes: HUgn10815
    ECgene: CPLX1 H-InvDB: CPLX1

    Other Databases showing CPLX1 gene

    (According to HUGE)
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    Specialized Databases showing CPLX1 gene

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for CPLX1 Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for CPLX1 gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    		Patent Information for CPLX1 gene:
    Search GeneIP for patents involving CPLX1

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