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

OCLM Gene

protein-coding   GIFtS: 35
GCID: GC01P186369

oculomedin

 Explore 3 diseases affiliated with
OCLM via our new
 Human Malady Compendium 
Biological research products
for OCLM
    

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

Aliases
Oculomedin1
TISR2 3
Trabecular Meshwork Inducible Stretch Response Protein2
Trabecular Meshwork-Inducible Stretch Response Protein3

External Ids:    HGNC: 81031   Entrez Gene: 108962   Ensembl: ENSG000002621807   OMIM: 6043015   UniProtKB: Q9Y5M63   

Export aliases for OCLM gene to outside databases

Previous GC identifers: GC01P183895 GC01P181797 GC01P182889 GC01U900851 GC01P183608 GC01P183101 GC01P184636


(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 OCLM:
The protein encoded by this gene is induced by cyclic mechanical stretching in trabecular cells of the eye and it is
also expressed in retina. This protein may play a role in trabecular meshwork function and the development of
glaucoma. (provided by RefSeq, Jul 2008)




(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_000001.10  NC_018912.1  NT_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the OCLM gene promoter:
         HFH-3   TBP   AML1a   Nkx2-5   C/EBPalpha   FOXI1   CHOP-10   TFIID   Zic3   Pax-4a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidOCLM promoter sequence
   Search SABiosciences Chromatin IP Primers for OCLM

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


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

Entrez Gene cytogenetic band: 1q25   Ensembl cytogenetic band:  1q31.1   HGNC cytogenetic band: 1q25

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

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P186369:  view genomic region     (about GC identifiers)

Start:
186,369,704 bp from pter      End:
186,370,587 bp from pter
Size:
884 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: TISR_HUMAN, Q9Y5M6 (See protein sequence)
Recommended Name: Oculomedin  
Size: 44 amino acids; 5321 Da
Secondary accessions: Q4G0F9

Explore the universe of human proteins at neXtProt for OCLM: NX_Q9Y5M6

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9Y5M6

  • OCLM Protein expression data from MOPED and PaxDb: --
    REFSEQ proteins: NP_071770.1  
    ENSEMBL proteins: 
     ENSP00000460371  

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

    ProtoNet protein and cluster: Q9Y5M6


    (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

    miRNA
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    (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 OCLM

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007601visual perception TAS10362512


    OCLM for ontologies           About GeneDecksing



    (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
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    (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 OCLM gene: 
    NM_022375.3  

    Unigene Cluster for OCLM:

    Oculomedin
    Hs.679230
    Unigene Representative Sequence: BC069096
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000574641(uc001gry.3)

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    Additional cDNA sequence: 

    BC069096.1 BC093987.1 BC093989.1 

    1 DOTS entry:

    DT.99949122 

    4 AceView cDNA sequences:

    BF964361 CD299370 AW851405 BF964342 

    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

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

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

    About this image
    Genevestigator expression for OCLM

    SOURCE GeneReport for Unigene cluster: Hs.679230

    UniProtKB/Swiss-Prot: TISR_HUMAN, Q9Y5M6
    Tissue specificity: Expressed in eye trabeculum; also expressed in retina

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    In Situ
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    (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 OCLM (if available)
    TreeFam Gene Tree for OCLM (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (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

    10/59 NCBI SNPs in OCLM are shown (see all 59    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs758485961,2
    --186367728(+) GGTGTG/CAAGAT 4 -- int1 us2k12Minor allele frequency- C:0.06CSA WA 119
    rs27371661,2
    C,H--186367757(+) TATTTT/GGTGCC 4 -- int1 us2k14Minor allele frequency- G:0.00NS EA 386
    rs1831963341,2
    --186367813(+) TATACA/GTATTA 4 -- int1 us2k10--------
    rs1874867381,2
    --186368001(+) GGAAAA/GCAAAT 4 -- int1 us2k10--------
    rs1508982631,2
    --186368205(+) TTTTGC/TGTATC 4 -- int1 us2k10--------
    rs1394349711,2
    --186368253(+) GATACA/GTCATC 4 -- int1 us2k10--------
    rs1929293411,2
    --186368277(+) TATCTA/GTATTT 4 -- int1 us2k10--------
    rs118053021,2
    C,F,H,--186368523(+) TTTTTT/CAGAGA 4 -- int1 us2k14Minor allele frequency- C:0.20NA EA 244
    rs358725061,2
    C,--186368662(+) AACAC-/TTTATCA 4 -- int1 us2k10--------
    rs712978341,2
    C--186368663(-) TTTGAAA/-TAGTG 4 -- int1 us2k11Minor allele frequency- -:0.50NA 2

    HapMap Linkage Disequilibrium report for OCLM (186369704 - 186370587 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for OCLM: --

    SABiosciences Cancer Mutation PCR Assays
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    (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

    OCLM for disorders           About GeneDecksing

    OMIM gene information: 604301    OMIM disorders: --

    3 diseases for OCLM:    About MalaCards
    open-angle glaucoma    glaucoma    primary open angle glaucoma


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

    1. A novel gene (oculomedin) induced by mechanical stretching in human trabecular cells of the eye. (PubMed id 10362512)1, 2, 3, 9 Sato Y.... Ohtsuki H. (1999)
    2. 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)
    3. Protein expression, genomic structure, and polymorphisms of oculomedin. (PubMed id 12868032)1, 9 Fujiwara N....Ohtsuki H. (2003)
    4. Absence of trabecular meshwork-inducible stretch response (TISR)/oculomedin gene and proximal promoter mutation in primary open angle glaucoma patients. (PubMed id 11129344)1, 9 Leung Y.F....Pang C.P. (2000)
    5. Evaluation of the Oculomedin gene in the etiology of primary open angle and exfoliative glaucoma. (PubMed id 12655282)1 Jansson M....Wadelius C. (2003)
    6. 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)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    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: 10896 HGNC: 8103 AceView: OCLM Ensembl:ENSG00000262180 euGenes: HUgn10896
    ECgene: OCLM H-InvDB: OCLM

    (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 OCLM Pharmacogenomics, SNPs, Pathways

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

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



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    About This Section

     
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