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

SCGB1D1 Gene

protein-coding   GIFtS: 47
GCID: GC11P061957

secretoglobin, family 1D, member 1

 Explore 6 diseases affiliated with
SCGB1D1 via our new
 Human Malady Compendium 
Biological research products
for SCGB1D1
    

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

Aliases
Secretoglobin, Family 1D, Member 11 2     Lipophilin-A3
LIPA1 2     Prostatein-Like Lipophilin A2
LPHA1 2     Secretoglobin Family 1D Member 12
MGC719581     LIPHA3
LPNA2     Lipophilin-A3
Lipophilin A (Uteroglobin Family Member)2     

External Ids:    HGNC: 183951   Entrez Gene: 106482   Ensembl: ENSG000001685157   OMIM: 6150605   UniProtKB: O959683   

Export aliases for SCGB1D1 gene to outside databases

Previous GC identifers: GC11P064471 GC11P063533 GC11P062208 GC11P061733 GC11P061714 GC11P058286


(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 SCGB1D1:
The protein encoded by this gene is a member of the lipophilin subfamily, part of the uteroglobin superfamily, and is
an ortholog of prostatein, the major secretory glycoprotein of the rat ventral prostate gland. This gene product
represents one component of a heterodimeric molecule present in human tears whose elution profile is consistent with
prostatein, a tetrameric molecule composed of three peptide components in heterodimers. Assuming that human
lipophilins are the functional counterparts of prostatein, they may be transcriptionally regulated by steroid
hormones, with the ability to bind androgens, other steroids and possibly bind and concentrate estramustine, a
chemotherapeutic agent widely used for prostate cancer. Although the gene has been reported to be on chromosome 15,
this sequence appears to be from a cluster of genes on chromosome 11 that includes mammaglobin 2. (provided by RefSeq,
Jul 2008)

UniProtKB/Swiss-Prot: SG1D1_HUMAN, O95968
Function: May bind androgens and other steroids, may also bind estramustine, a chemotherapeutic agent used for prostate
cancer. May be under transcriptional regulation of steroid hormones




(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_000011.9  NC_018922.1  NT_167190.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SCGB1D1 gene promoter:
         TBP   MEF-2A   NRSF form 1   aMEF-2   NRSF form 2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSCGB1D1 promoter sequence
   Search SABiosciences Chromatin IP Primers for SCGB1D1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SCGB1D1


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

Entrez Gene cytogenetic band: 11q13   Ensembl cytogenetic band:  11q12.3   HGNC cytogenetic band: 11q13

SCGB1D1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SCGB1D1 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P061957:  view genomic region     (about GC identifiers)

Start:
61,957,688 bp from pter      End:
61,961,011 bp from pter
Size:
3,324 bases      Orientation:
plus strand

(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: SG1D1_HUMAN, O95968 (See protein sequence)
Recommended Name: Secretoglobin family 1D member 1 precursor  
Size: 90 amino acids; 9898 Da
Subunit: Heterodimer of a lipophilin A and a lipophilin C (mammaglobin B) monomer associated head to head
Subcellular location: Secreted (Potential)
Mass spectrometry: Mass=7574.69; Method=Electrospray; Range=22-90; Source=PubMed:9720917;

Explore the universe of human proteins at neXtProt for SCGB1D1: NX_O95968

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O95968

  • SCGB1D1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_006543.1  
    ENSEMBL proteins: 
     ENSP00000303070  

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005615extracellular space TAS10066439


    SCGB1D1 for ontologies           About GeneDecksing



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

    SCGB1D1 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR016126 Secretoglobin
     IPR006038 Uteroglobin-like_superfam
     IPR006039 Uteroglobin-like_fam

    Graphical View of Domain Structure for InterPro Entry O95968

    ProtoNet protein and cluster: O95968

    UniProtKB/Swiss-Prot: SG1D1_HUMAN, O95968
    Similarity: Belongs to the secretoglobin family. Lipophilin subfamily


    (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: SG1D1_HUMAN, O95968
    Function: May bind androgens and other steroids, may also bind estramustine, a chemotherapeutic agent used for prostate
    cancer. May be under transcriptional regulation of steroid hormones

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    1 GenomeRNAi human phenotype for SCGB1D1:
     Decreased G3BP1 protein expres 


    (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 SCGB1D1

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    1 Interacting protein for SCGB1D1 (O959683 ENSP000003030704) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SCGB2A1O755563, ENSP000002449304I2D: score=1 STRING: ENSP00000244930
    About this table

    (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 SCGB1D1
    Search CenterWatch for drugs/clinical trials and news about SCGB1D1 / SG1D1 

    (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,
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    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 SCGB1D1 gene: 
    NM_006552.1  

    Unigene Cluster for SCGB1D1:

    Secretoglobin, family 1D, member 1
    Hs.202686  [show with all ESTs]
    Unigene Representative Sequence: CB987582
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000306238(uc001nsz.1)

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    Clone
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    Additional cDNA sequence: 

    AJ224171.1 BC062693.1 BC069170.1 BC069289.1 

    1 DOTS entry:

    DT.92037292 

    14 AceView cDNA sequences:

    NM_006552 CA946451 BC069170 CK430411 CD723001 BC069289 AJ224171 CB957594 
    CB987851 CB956606 CD722937 BC062693 CK431208 CB987582 

    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

    SCGB1D1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AGGCTGTCGG

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

    About this image
    See SCGB1D1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SCGB1D1

    SOURCE GeneReport for Unigene cluster: Hs.202686

    UniProtKB/Swiss-Prot: SG1D1_HUMAN, O95968
    Tissue specificity: Expressed in lachrymal gland, thymus, kidney, testis, ovary and salivary gland

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SCGB1D1

    (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
      --

    ENSEMBL Gene Tree for SCGB1D1 (if available)
    TreeFam Gene Tree for SCGB1D1 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SCGB1D1 gene
    SCGB1D22  SCGB1D42  
    2 SIMAP similar genes for SCGB1D1 using alignment to 1 protein entry:     SG1D1_HUMAN:
    SCGB1D4    SCGB1D2

    SCGB1D1 for paralogs           About GeneDecksing



    (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

    10/124 NCBI SNPs in SCGB1D1 are shown (see all 124    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs112309721,2
    C,F,A,--61955940(+) GAGACG/AGGGTT 1 -- us2k14Minor allele frequency- A:0.43NA WA CSA 7
    rs1875509021,2
    --61955942(+) GACGGC/GGTTTC 1 -- us2k10--------
    rs1915403461,2
    --61955965(+) AGACTA/GGTCTC 1 -- us2k10--------
    rs1382577191,2
    --61955995(+) ATCCAC/TCCGCC 1 -- us2k10--------
    rs38250331,2
    C,F,A,--61956010(-) ACTTTA/GGGAGG 1 -- us2k14Minor allele frequency- G:0.25NA WA 8
    rs1829929901,2
    --61956053(+) GCCAGA/TCCTGG 1 -- us2k10--------
    rs1158180201,2
    --61956150(+) ACAAAC/TGAGAA 1 -- us2k11Minor allele frequency- T:0.01WA 118
    rs1875184611,2
    --61956199(+) AGCCCA/GTAGAC 1 -- us2k10--------
    rs757572941,2
    --61956242(+) CCACTG/AGACCT 1 -- us2k11Minor allele frequency- A:0.01NA 120
    rs122235481,2
    C,F,--61956273(+) GCAGAG/AGTGGC 1 -- us2k12Minor allele frequency- A:0.29NA EA 240

    HapMap Linkage Disequilibrium report for SCGB1D1 (61957688 - 61961011 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for SCGB1D1: --

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    (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

    SCGB1D1 for disorders           About GeneDecksing

    OMIM gene information: 615060    OMIM disorders: --

    6 diseases for SCGB1D1:    About MalaCards
    prostate cancer    prostatitis    patellofemoral pain syndrome    intracranial hypotension
    paine syndrome    lung cancer

    2 diseases from the University of Copenhagen DISEASES database for SCGB1D1:
    Patellofemoral pain syndrome     Intracranial hypotension

    1 Novoseek disease relationship for SCGB1D1 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    tumors 0 1 16120813 (1)


    Export disorders for SCGB1D1 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 SCGB1D1 gene, integrated from 9 sources (see all 11):
    (articles sorted by number of sources associating them with SCGB1D1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Lipophilins: human peptides homologous to rat prostatein. (PubMed id 10066439)1, 2, 3, 9 Zhao C.... Lehrer R.I. (1999)
    2. Lipophilin, a novel heterodimeric protein of human tears. (PubMed id 9720917)1, 2, 3, 9 Lehrer R.I....Glasgow B.J. (1998)
    3. Update of the human secretoglobin (SCGB) gene superfa mily and an example of 'evolutionary bloom' of androgen-binding protein genes w ithin the mouse Scgb gene superfamily. (PubMed id 22155607)1, 3 Jackson B.C....Vasiliou V. (2011)
    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. 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. (2002)
    6. Evaluation of lipophilins as determinants of tumor cell response to estramustine. (PubMed id 16120813)9 Tucker J.M....Tew K.D. (2005)
    7. Dysregulated secretoglobin expression in human lung cancers. (PubMed id 12826312)9 Sjodin A....Hedman H. (2003)
    8. The Neisseria meningitidis capsule is important for intracellular survival in human cells. (PubMed id 17470547)9 Spinosa M.R....Bucci C. (2007)
    9. Immunohistochemical analysis of secretoglobin SCGB 2A1 expression in human ocular glands and tissues. (PubMed id 16395610)9 Stoeckelhuber M....Klug J. (2006)
    10. Secretoglobin 2A1 is under selective androgen control mediated by a peculiar binding site for Sp family transcription factors. (PubMed id 16020486)9 Xiao F....Klug J. (2005)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 10648 HGNC: 18395 AceView: SCGB1D1 Ensembl:ENSG00000168515 euGenes: HUgn10648
    ECgene: SCGB1D1 H-InvDB: SCGB1D1

    (According to HUGE)
    About This Section
      --

    (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 SCGB1D1 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for SCGB1D1 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for SCGB1D1 gene:
    Search GeneIP for patents involving SCGB1D1

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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    About This Section

     
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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 27 Apr 2013

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    VWF
    (GIFTS: 73)
    von Willebrand factor
    GIFtS Group
    The GeneCards human gene database gene index: 1 3 5 6 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 


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