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

SLURP1 Gene

protein-coding   GIFtS: 51
GCID: GC08M143820

Secreted LY6/PLAUR Domain Containing 1

Microbiology & Infectious Diseases Congress
  See 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)
About This Section

Aliases
Secreted LY6/PLAUR Domain Containing 11 2     ARS(Component B)-81/S2 3
ARS Component B1 3     MDM2 5
Lymphocyte Antigen 6-Like Secreted1 2     ArsB2
Anti-Neoplastic Urinary Protein2 3     LY6LS2
ANUP2 3     Secreted Ly-6/UPAR-Related Protein 12
ARS2 3     Secreted Ly6/UPAR Related Protein 12
SLURP-12 3     

External Ids:    HGNC: 187461   Entrez Gene: 571522   Ensembl: ENSG000001262337   OMIM: 6061195   UniProtKB: P550003   

Export aliases for SLURP1 gene to outside databases

Previous GC identifer: GC08M139075


(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 SLURP1 Gene:
The protein encoded by this gene is a member of the Ly6/uPAR family but lacks a GPI-anchoring signal sequence. It
is thought that this secreted protein contains antitumor activity. Mutations in this gene have been associated
with Mal de Meleda, a rare autosomal recessive skin disorder. This gene maps to the same chromosomal region as
several members of the Ly6/uPAR family of glycoprotein receptors. (provided by RefSeq, Jul 2008)

GeneCards Summary for SLURP1 Gene: 
SLURP1 (secreted LY6/PLAUR domain containing 1) is a protein-coding gene. Diseases associated with SLURP1 include meleda disease, and prostate carcinoma in situ. GO annotations related to this gene include cytokine activity. An important paralog of this gene is LYPD2.

UniProtKB/Swiss-Prot: SLUR1_HUMAN, P55000
Function: Has an antitumor activity. Was found to be a marker of late differentiation of the skin. Implicated in
maintaining the physiological and structural integrity of the keratinocyte layers of the skin

Gene Wiki entry for SLURP1 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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000008.10  NC_018919.2  NT_008046.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLURP1 gene promoter:
         GR   p53   GR-beta   Nkx2-5   Tal-1beta   AP-2gamma   C/EBPalpha   GR-alpha   ITF-2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLURP1 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLURP1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLURP1


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

Entrez Gene cytogenetic band: 8q24.3   Ensembl cytogenetic band:  8q24.3   HGNC cytogenetic band: 8q24.3

SLURP1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLURP1 gene location

GeneLoc information about chromosome 8         GeneLoc Exon Structure

GeneLoc location for GC08M143820:  view genomic region     (about GC identifiers)

Start:
143,822,362 bp from pter      End:
143,823,829 bp from pter
Size:
1,468 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: SLUR1_HUMAN, P55000 (See protein sequence)
Recommended Name: Secreted Ly-6/uPAR-related protein 1 precursor  
Size: 103 amino acids; 11186 Da
Subunit: Homodimer
Subcellular location: Secreted
Caution: It is not certain that ARS and ANUP are identical proteins
Secondary accessions: Q53YJ6 Q6PUA6 Q92483

Explore the universe of human proteins at neXtProt for SLURP1: NX_P55000

Explore proteomics data for SLURP1 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_P55000

  • SLURP1 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    SLURP1 Protein Expression
    REFSEQ proteins: NP_065160.1  
    ENSEMBL proteins: 
     ENSP00000246515  

    Human Recombinant Protein Products for SLURP1: 
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    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
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    Cloud-Clone Corp. Proteins for SLURP1 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region NAS14721776
    GO:0005615extracellular space IEA--

    SLURP1 for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    3 InterPro protein domains:
     IPR016054 LY6_UPA_recep-like
     IPR027103 SLURP1
     IPR001526 LY6_UPAR

    Graphical View of Domain Structure for InterPro Entry P55000

    ProtoNet protein and cluster: P55000

    1 Blocks protein domain: IPB001526 CD59 antigen

    UniProtKB/Swiss-Prot: SLUR1_HUMAN, P55000
    Similarity: Contains 1 UPAR/Ly6 domain


    SLURP1 for domains           About GeneDecksing


    (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,
    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, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: SLUR1_HUMAN, P55000
    Function: Has an antitumor activity. Was found to be a marker of late differentiation of the skin. Implicated in
    maintaining the physiological and structural integrity of the keratinocyte layers of the skin
    Induction: Regulated by retinoic acid, EGF and IFNG/IFN-gamma

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005125cytokine activity NAS8742060
         
    SLURP1 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for SLURP1:
     Increased gamma-H2AX phosphory 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for SLURP1 
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    Inhib. RNA
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    (Pathways according to EMD Millipore, 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 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for SLURP1

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001775cell activation NAS11285253
    GO:0007155cell adhesion TAS14506129

    SLURP1 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    SLURP1 for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for SLURP1 (SLUR1)

    7 Novoseek inferred chemical compound relationships for SLURP1 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    anup 96.5 9 8742060 (3), 9920854 (1), 11227487 (1), 15165708 (1)
    antimonite 83.2 1 9271073 (1)
    arsenate 68.9 2 11931390 (1), 9271073 (1)
    arsenite 67.5 4 11931390 (2), 17061211 (1), 9271073 (1)
    norepinephrine 11.4 3 2154750 (1), 10779380 (1)
    steroid 6.98 1 16707768 (1)
    testosterone 0 1 16707768 (1)

    Search CenterWatch for drugs/clinical trials and news about SLURP1 / SLUR1

    (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,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for SLURP1 gene: 
    NM_020427.2  

    Unigene Clusters for SLURP1:

    Secreted LY6/PLAUR domain containing 1
    Hs.103505  [show with all ESTs], Hs.676358
    Unigene Representative Sequences: BQ027886, NM_020427
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000246515(uc003ywy.3)
    Congresses - knowledge worth sharing:  
    European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) 10 - 13 May 2014

    miRNA
    Products:
         
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    Inhib. RNA
    Products:
         
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat SLURP1
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SLURP1

    Additional mRNA sequence: 

    AY579079.1 AY579080.1 BC069292.1 

    1 DOTS entry:

    DT.97805489 

    10 AceView cDNA sequences:

    BX107730 AY579080 NM_020427 BC069292 AI092857 AY579079 BQ027921 BQ027886 
    BQ188001 CA433583 

    GeneLoc Exon Structure


    (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

    SLURP1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: --
    SLURP1 Expression
    About this image


    See SLURP1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLURP1

    SOURCE GeneReport for Unigene clusters: Hs.103505 Hs.676358

    UniProtKB/Swiss-Prot: SLUR1_HUMAN, P55000
    Tissue specificity: Granulocytes. Expressed in skin. Predominantly expressed in the granular layer of skin,
    notably the acrosyringium. Identified in several biological fluids such as sweat, saliva, tears, plasma and urine

        SABiosciences Expression via Pathway-Focused PCR Array including SLURP1: 
              Inflammatory Response & Autoimmunity 384HT in human mouse rat

    Primer
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLURP1

    (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 chordates.

    Orthologs for SLURP1 gene from 3/9 species (see all 9)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Slurp11 , 5 secreted Ly6/Plaur domain containing 11, 5 78.55(n)1
    69.31(a)1
      15 (34.26 cM)5
    572771  NM_020519.11  NP_065265.11 
     747266445 
    chicken
    (Gallus gallus)
    Aves SLURP16
    secreted LY6/PLAUR domain containing 1
    31(a)
    1 ↔ 1
    2(147883994-147890790)
    lizard
    (Anolis carolinensis)
    Reptilia SLURP16
    Uncharacterized protein
    33(a)
    1 ↔ 1
    GL343222.1(2349367-2350271)


    ENSEMBL Gene Tree for SLURP1 (if available)
    TreeFam Gene Tree for SLURP1 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLURP1 gene
    LYPD22  
    1 SIMAP similar gene for SLURP1 using alignment to 1 protein entry:     SLUR1_HUMAN:
    LYPD2

    SLURP1 for paralogs           About GeneDecksing



    (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) 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

    10/114 SNPs in SLURP1 are shown (see all 114)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 8 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    VAR_0328714
    Mal de Meleda (MDM)4--see VAR_0328712 W R mis40--------
    VAR_0328724
    Mal de Meleda (MDM)4--see VAR_0328722 R H mis40--------
    VAR_0328734
    Mal de Meleda (MDM)4--see VAR_0328732 C R mis40--------
    VAR_0328754
    Mal de Meleda (MDM)4--see VAR_0328752 C Y mis40--------
    rs289378881,2,4
    CMal de Meleda (MDM)4 untested1144096802(-) GCATCA/C/GGGGCC 3 R G mis10--------
    rs289378891,2
    Cpathogenic1144097988(-) GAGCAA/CTGGCC 2 M L mis10--------
    rs1436484651,2
    --144096072(+) CCTCCA/GCTAAT 1 -- ds50010--------
    rs349564121,2
    C,F,H--144096213(+) GTATCC/TACCCT 1 -- ds500120Minor allele frequency- T:0.22NS EA NA CSA WA 2344
    rs1823280361,2
    --144096231(+) AAGTGA/GATGCC 1 -- ds50010--------
    rs47363211,2
    C,F,A--144096379(+) GGGCCC/TAGGAG 1 -- ds500111Minor allele frequency- T:0.26NA CSA WA EA 508

    HapMap Linkage Disequilibrium report for SLURP1 (143822362 - 143823829 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 9 variations for SLURP1:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2661137CNV Deletion23128226
    esv2737925CNV Deletion23290073
    nsv891638CNV Loss21882294
    dgv7917n71CNV Loss21882294
    dgv7910n71CNV Loss21882294
    dgv7915n71CNV Loss21882294
    nsv831485CNV Loss17160897
    nsv891639CNV Gain21882294
    nsv831486CNV Gain17160897


    Human Gene Mutation Database (HGMD): SLURP1
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing SLURP1
    DNA2.0 Custom Variant and Variant Library Synthesis for SLURP1

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 606119   
    OMIM disorders: 248300  
    UniProtKB/Swiss-Prot: SLUR1_HUMAN, P55000
  • Mal de Meleda (MDM) [MIM:248300]: A rare autosomal recessive skin disorder, characterized by diffuse
    transgressive palmoplantar keratoderma with keratotic lesions extending onto the dorsa of the hands and the feet
    (transgrediens). Patients may have hyperhidrosis. Other features include perioral erythema, lichenoid plaques on
    the knees and the elbows, and nail abnormalities. Note=The disease is caused by mutations affecting the gene
    represented in this entry

  • 14 diseases for SLURP1:    About MalaCards
    meleda disease    prostate carcinoma in situ    palmoplantar keratosis    hydranencephaly
    keratoderma    keratosis    skin disease    kaposi's sarcoma
    cataract    hepatitis b    sarcoma    colon cancer
    prostatitis    hepatitis

    2 diseases from the University of Copenhagen DISEASES database for SLURP1:
    Palmoplantar keratosis     Hydranencephaly

    SLURP1 for disorders           About GeneDecksing

    4 Novoseek inferred disease relationships for SLURP1 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    mal de meleda 98.5 26 12535203 (3), 12950349 (3), 11872406 (2), 14506129 (2) (see all 16)
    keratoderma palmoplantar 90.9 5 19396877 (1), 12603845 (1), 16865292 (1), 17008884 (1) (see all 5)
    skin diseases 47.6 2 19396877 (1), 14506129 (1)
    tumors 0 4 10233778 (1), 19396877 (1), 15909066 (1), 9920854 (1)

    Human Genome Epidemiology (HuGE) Navigator: SLURP1 (1 document)

    Export disorders for SLURP1 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

    PubMed articles for SLURP1 gene, integrated from 9 sources (see all 56):
    (articles sorted by number of sources associating them with SLURP1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Mutations in the gene encoding SLURP-1 in Mal de Meleda. (PubMed id 11285253)1, 2, 3, 9 Fischer J.... Prud'homme J.-F. (2001)
    2. Structural and phylogenetic characterization of human SLURP-1, the first secreted mammalian member of the Ly-6/uPAR protein superfamily. (PubMed id 10211827)1, 2, 3, 9 Andermann K.... Nehls M. (1999)
    3. Partial N-terminal amino acid sequence of the anti-neoplastic urinary protein (ANUP) and the anti-tumour effect of the N-terminal nonapeptide of the unique cytokine present in human granulocytes. (PubMed id 8742060)1, 2, 9 Ridge R.J. and Sloane N.H. (1996)
    4. ARS component B: structural characterization, tissue expression and regulation of the gene and protein (SLURP-1) associated with Mal de Meleda. (PubMed id 14721776)1, 2, 9 Mastrangeli R.... Papoian R. (2003)
    5. Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates. (PubMed id 12483299)1, 2, 9 Eckl K.M.... Hennies H.C. (2003)
    6. Biological effects of SLURP-1 on human keratinocytes. (PubMed id 16354194)1, 2 Arredondo J.... Grando S.A. (2005)
    7. Heterozygous manifestations in female carriers of Mal de Meleda. (PubMed id 14756676)1, 2 Mokni M.... Abdelhak S. (2004)
    8. 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)
    9. SLURP1 is a late marker of epidermal differentiation and is absent in Mal de Meleda. (PubMed id 17008884)2, 9 Favre B.... Hohl D. (2007)
    10. Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda. (PubMed id 14506129)1, 9 Chimienti F....Hohl D. (2003)

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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: 57152 HGNC: 18746 AceView: ARS Ensembl:ENSG00000126233 euGenes: HUgn57152
    ECgene: SLURP1 H-InvDB: SLURP1

    (According to HUGE)
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    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
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    NameDescription
    PharmGKB entry for SLURP1 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for SLURP1 Genetics and Cytogenetics in Oncology and Haematology

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    Patent Information for SLURP1 gene:
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