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

SCRN1 Gene

protein-coding   GIFtS: 52
GCID: GC07M029926

secernin 1
 Explore 6 diseases affiliated with
SCRN1 via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for SCRN1    

Aliases
for SCRN1 gene

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section
Aliases
Secernin 11 2
KIAA01931 3
SES12
Secernin-11

External Ids:    HGNC: 221921   Entrez Gene: 98052   Ensembl: ENSG000001361937   OMIM: 6149655   UniProtKB: Q127653   

Export aliases for SCRN1 gene to outside databases

Previous GC identifers: GC07M029703 GC07M029732


Summaries
for SCRN1 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 SCRN1:
This gene likely encodes a member of the secernin family of proteins. A similar protein in rat functions in regulation
of exocytosis in mast cells. Alternatively spliced transcript variants have been described. (provided by RefSeq, Mar
2009)

UniProtKB/Swiss-Prot: SCRN1_HUMAN, Q12765
Function: Regulates exocytosis in mast cells. Increases both the extent of secretion and the sensitivity of mast cells
to stimulation with calcium (By similarity)

Gene Wiki entry for SCRN1


Genomic Views
for SCRN1 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_000007.13  NC_018918.1  NT_007819.17  NT_079592.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SCRN1 gene promoter:
         AML1a   POU2F1   POU2F1a   GATA-1   GATA-2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 4): SCRN1 promoter sequence
   Search SABiosciences Chromatin IP Primers for SCRN1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SCRN1


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

Entrez Gene cytogenetic band: 7p14.3-p14.1   Ensembl cytogenetic band:  7p14.3   HGNC cytogenetic band: 7p14.3-p14.1

SCRN1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SCRN1 gene location

GeneLoc information about chromosome 7         GeneLoc Exon Structure

GeneLoc location for GC07M029926:  view genomic region     (about GC identifiers)

Start:
 29,959,719 bp from pter      End:
 30,029,905 bp from pter
Size:
 70,187 bases      Orientation:
 minus strand

1 alternative location:
Chr7-,CRA_TCAG 30,009,542-30,079,734     

Proteins
for SCRN1 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: SCRN1_HUMAN, Q12765 (See protein sequence)
Recommended Name: Secernin-1  
Size: 414 amino acids; 46382 Da
Subcellular location: Cytoplasm (By similarity)
Miscellaneous: 'Secern' is an archaic English term meaning 'secrete'
Sequence caution: Sequence=BAA12106.2; Type=Erroneous initiation;
Secondary accessions: A8K0E9 B4DHM0 B4DIP5 C9JPG0 Q25QX7 Q8IWD1
Alternative splicing: 3 isoforms:  Q12765-1   Q12765-2   Q12765-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SCRN1: NX_Q12765

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q12765

    • SCRN1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (4 alternative transcripts): 
    NP_001138985.1  NP_001138986.1  NP_001138987.1  NP_055581.3  

    ENSEMBL proteins: 
     ENSP00000242059   ENSP00000414245   ENSP00000386872   ENSP00000388942   ENSP00000413184  
     ENSP00000406289   ENSP00000387052   ENSP00000409068   ENSP00000407460  

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    Novus Biologicals SCRN1 Protein
    Novus Biologicals SCRN1 Lysates
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    Browse ProSpec Recombinant Proteins
    Uscn Proteins for SCRN1

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA10942595
    GO:0005737cytoplasm IEA--
    GO:0031965nuclear membrane IDA10942595


    SCRN1 for ontologies           About GeneDecksing



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    Protein Domains /
    Families
    for SCRN1 gene

    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    SCRN1 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR005322 Peptidase_C69

    Graphical View of Domain Structure for InterPro Entry Q12765

    ProtoNet protein and cluster: Q12765

    UniProtKB/Swiss-Prot: SCRN1_HUMAN, Q12765
    Similarity: Belongs to the peptidase C69 family. Secernin subfamily


    Function
    for SCRN1 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: SCRN1_HUMAN, Q12765
    Function: Regulates exocytosis in mast cells. Increases both the extent of secretion and the sensitivity of mast cells
    to stimulation with calcium (By similarity)

    miRNA
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    hsa-miR-140-5p hsa-miR-2052 hsa-miR-3938 hsa-miR-19b-2* hsa-miR-1260b hsa-miR-605 hsa-miR-1258 hsa-let-7a-2*
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    OriGene shRNA RFP: SCRN1
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    Gene Editing
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    Clone
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    Cell Line
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    Search LifeMap BioReagents cell lines for SCRN1

    In Situ Assay
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    Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003674molecular_function ND--
    GO:0016805dipeptidase activity IEA--


    SCRN1 for ontologies           About GeneDecksing



    Pathways & Interactions
    for SCRN1 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



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SCRN1

    STRING Interaction Network Preview (showing 2 interactants - click image to see more details)

    5 Interacting proteins for SCRN1 (Q127653 ENSP000004074604) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    HGSO149643, ENSP000003312014I2D: score=1 STRING: ENSP00000331201
    DDA1Q9BW613I2D: score=1 
    DLG4P783523I2D: score=1 
    SOD2P041793I2D: score=1 
    UBCENSP000003448184STRING: ENSP00000344818
    About this table

    Gene Ontology (GO): 2 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006508proteolysis IEA--
    GO:0006887exocytosis ISS--


    SCRN1 for ontologies           About GeneDecksing



    Drugs & Compounds
    for SCRN1 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 SCRN1

    1 HMDB Compound for SCRN1    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--
    Search CenterWatch for drugs/clinical trials and news about SCRN1 

    Transcripts
    for SCRN1 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 SCRN1 gene (4 alternative transcripts): 
    NM_001145513.1  NM_001145514.1  NM_001145515.1  NM_014766.4  

    Unigene Cluster for SCRN1:

    Secernin 1
    Hs.520740  [show with all ESTs]
    Unigene Representative Sequence: NM_001145513
    10 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000242059(uc011jzw.2 uc010kvp.3 uc011jzx.2 uc011jzy.2 uc003tak.3 uc011kaa.2)
    ENST00000425819 ENST00000409497 ENST00000434476 ENST00000421434 ENST00000494620
    ENST00000438497 ENST00000409570 ENST00000426154(uc011jzz.2) ENST00000416113


    miRNA
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    hsa-miR-140-5p hsa-miR-2052 hsa-miR-3938 hsa-miR-19b-2* hsa-miR-1260b hsa-miR-605 hsa-miR-1258 hsa-let-7a-2*
    Browse SwitchGear 3'UTR luciferase reporter plasmids
    Inhib. RNA
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    OriGene shRNA RFP: SCRN1
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    Clone
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    Additional cDNA sequence: 

    AB071705.1 AK289514.1 AK293462.1 AK294891.1 AK295172.1 AK295713.1 AK295800.1 BC040492.1 
    D83777.2 

    11 DOTS entries:

    DT.452456  DT.100726108  DT.91770594  DT.97869709  DT.121094573  DT.75156026  DT.121094584  DT.121094594 
    DT.101961899  DT.121094619  DT.452455 

    24/360 AceView cDNA sequences (see all 360):

    AI418855 AI923221 N24779 AI357913 AW662116 CB306531 AA987271 AI860396 
    BU625648 AI332576 BQ071539 AA621221 AU130411 AI277293 AU130607 AI298253 
    CA944792 AA181639 AU123282 AA582306 AI375759 AA169219 BM679325 CD513066 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for SCRN1    About this scheme

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


    ECgene alternative splicing isoforms for SCRN1

    Expression
    for SCRN1 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

    SCRN1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TAGTCTTAAC

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

    SCRN1 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    4 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    EyeInner Nuclear LayerMature Horizontal CellsHorizontal, Retina
    EyeInner Nuclear LayerMature Rod Bipolar CellsBipolar, Retina
    KidneyS-shaped BodyKidney
    Neural TubeMesencephalic Ventricular ZoneNeural Tube
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See SCRN1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SCRN1

    SOURCE GeneReport for Unigene cluster: Hs.520740
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    In Situ
    Assay Products:     
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    Orthologs
    for SCRN1 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 SCRN1 gene from 4/12 species (see all 12)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    chicken
    (Gallus gallus)    		 Aves SCRN11 secernin 1 75.44(n)
    80.43(a)    		   420635  XM_418734.3  XP_418734.3 
    lizard
    (Anolis carolinensis)    		 Reptilia SCRN16
    		 --
    		 78(a)
    		 1 ↔ 1
    		 6(35524800-35549420)
    African clawed frog
    (Xenopus laevis)    		 Amphibia Xl.180222 Xenopus laevis transcribed sequence with weak similarity more 75.51(n)    CD325975.1 
    fruit fly
    (Drosophila melanogaster)    		 Insecta CG100981 CG10098 44.12(n)
    29.41(a)    		   40851  NM_141437.3  NP_649694.1 


    ENSEMBL Gene Tree for SCRN1 (if available)
    TreeFam Gene Tree for SCRN1 (if available) 

    Paralogs
    for SCRN1 gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SCRN1 gene
    SCRN32  SCRN22  
    2 SIMAP similar genes for SCRN1 using alignment to 5 protein entries:     SCRN1_HUMAN (see all proteins):
    SCRN3    SCRN2

    SCRN1 for paralogs           About GeneDecksing



    Genomic Variants
    for SCRN1 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

    10/1094 NCBI SNPs in SCRN1 are shown (see all 1094)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr 7 posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs773848501,2
    		C,F,--29959234(+) CTGTGA/CATAGT 4 -- ds50013Minor allele frequency- C:0.07WA NA EA 358
    rs747119261,2
    		C,F,--29959308(+) CCCAGA/GAGTGG 4 -- ds50011Minor allele frequency- G:0.06WA 118
    rs102789901,2
    		C,F,A,H,--29959413(+) AGTACA/GTAAGG 4 -- ds50019Minor allele frequency- G:0.32NA WA CSA EA 370
    rs1417611781,2
    		--29959462(+) TTCTGA/GTTGTG 4 -- ds50010--------
    rs1506991061,2
    		C,--29959472(+) GTTTT-/TTGTTGTT 4 -- ds50010--------
    rs591757731,2
    		C--29959489(+) TTGTT-/GTTTTTGT 4 -- ds50010--------
    rs1883683171,2
    		--29959525(+) TGTGAA/GGTGAT 4 -- ds50010--------
    rs1454195041,2
    		--29959585(+) ACATGA/GTGCAA 4 -- ds50010--------
    rs171584731,2
    		C,F,H,--29959679(+) GCCCAC/TGTTTA 4 -- ds500128Minor allele frequency- T:0.06NA NS EA CSA WA 3322
    rs1922960121,2
    		--29959680(+) CCCACA/GTTTAT 4 -- ds50010--------

    HapMap Linkage Disequilibrium report for SCRN1 (29959719 - 30029905 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for SCRN1: --

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing SCRN1
    DNA2.0 Custom Variant and Variant Library Synthesis for SCRN1

    Disorders / Diseases
    for SCRN1 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
    SCRN1 for disorders           About GeneDecksing

    OMIM gene information: 614965    OMIM disorders: --

    6 diseases for SCRN1:    About MalaCards
    barrett's esophagus    synovial sarcoma    sarcoma    gastric cancer
    retinitis    schizophrenia

    Human Genome Epidemiology (HuGE) Navigator: SCRN1 (1 document)

    Export disorders for SCRN1 gene to outside databases

    Publications
    for SCRN1 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 SCRN1 gene, integrated from 9 sources (see all 24):
    (articles sorted by number of sources associating them with SCRN1)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of secernin 1 as a novel immunotherapy target for gastric cancer using the expression profiles of cDNA microarray. (PubMed id 16630140)1, 2, 9 Suda T.... Tahara H. (2006)
    2. Purification and identification of secernin, a novel cytosolic protein that regulates exocytosis in mast cells. (PubMed id 12221138)1, 3, 9 Way G....O'Sullivan A.J. (2002)
    3. 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)
    4. The DNA sequence of human chromosome 7. (PubMed id 12853948)1, 2 Hillier L.W.... Wilson R.K. (2003)
    5. Towards complete analysis of the platelet proteome. (PubMed id 11921445)1, 2 O'Neill E.E.... Hebestreit H.F. (2002)
    6. Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones. (PubMed id 12168954)1, 2 Nakajima D.... Nagase T. (2002)
    7. Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1. (PubMed id 8724849)1, 2 Nagase T.... Nomura N. (1996)
    8. SCRN1 is a novel marker for prognosis in colorectal c ancer. (PubMed id 20039278)1, 9 Miyoshi N....Mori M. (2010)
    9. Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration. (PubMed id 22360420)1 Martins-de-Souza D....Bahn S. (2012)
    10. A high-throughput approach for measuring temporal chan ges in the interactome. (PubMed id 22863883)1 Kristensen A.R....Foster L.J. (2012)

    External Searches for SCRN1 gene

    (in PubMed, OMIM, and NCBI Bookshelf)
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    Genome Databases showing SCRN1 gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9805 HGNC: 22192 AceView: SCRN1 Ensembl:ENSG00000136193 euGenes: HUgn9805
    ECgene: SCRN1 H-InvDB: SCRN1

    Other Databases showing SCRN1 gene

    (According to HUGE)
    About This Section
    HUGE: KIAA0193

    Specialized Databases showing SCRN1 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 SCRN1 Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for SCRN1 gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    		Patent Information for SCRN1 gene:
    Search GeneIP for patents involving SCRN1

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