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

PRAME Gene

protein-coding   GIFtS: 54
GCID: GC22M022890

preferentially expressed antigen in melanoma


(Previous symbol: MAPE)
 Explore 36 diseases affiliated with
PRAME via our new
 Human Malady Compendium 
Biological research products
for PRAME
    

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

Aliases
Preferentially Expressed Antigen In Melanoma1 2     Preferentially Expressed Antigen Of Melanoma2 3
MAPE1 2 3 5     OIP-42 3
OIP42 3 5     Cancer/Testis Antigen 1302
CT1301 2     Melanoma Antigen Preferentially Expressed In Tumors2
Opa-Interacting Protein 42 3     Opa-Interacting Protein OIP42

External Ids:    HGNC: 93361   Entrez Gene: 235322   Ensembl: ENSG000001856867   OMIM: 6060215   UniProtKB: P783953   

Export aliases for PRAME gene to outside databases

Previous GC identifers: GC22M019588 GC22M021214 GC22M020673 GC22M005860


(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 PRAME:
This gene encodes an antigen that is predominantly expressed in human melanomas and that is recognized by cytolytic T
lymphocytes. It is not expressed in normal tissues, except testis. This expression pattern is similar to that of other
CT antigens, such as MAGE, BAGE and GAGE. However, unlike these other CT antigens, this gene is also expressed in
acute leukemias. Five alternatively spliced transcript variants encoding the same protein have been observed for this
gene. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: PRAME_HUMAN, P78395
Function: Functions as a transcriptional repressor, inhibiting the signaling of retinoic acid through the retinoic acid
receptors RARA, RARB and RARG. Prevents retinoic acid-induced cell proliferation arrest, differentiation and apoptosis

Gene Wiki entry for PRAME


(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_000022.10  NC_018933.1  NT_011520.12  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the PRAME gene promoter:
         AML1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidPRAME promoter sequence
   Search SABiosciences Chromatin IP Primers for PRAME

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


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

Entrez Gene cytogenetic band: 22q11.22   Ensembl cytogenetic band:  22q11.22   HGNC cytogenetic band: 22q11.22

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

GeneLoc information about chromosome 22         GeneLoc Exon Structure

GeneLoc location for GC22M022890:  view genomic region     (about GC identifiers)

Start:
22,890,123 bp from pter      End:
22,901,768 bp from pter
Size:
11,646 bases      Orientation:
minus 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: PRAME_HUMAN, P78395 (See protein sequence)
Recommended Name: Melanoma antigen preferentially expressed in tumors  
Size: 509 amino acids; 57890 Da
Subunit: Interacts with RARA (via the ligand-binding domain); the interaction is direct and ligand (retinoic
acid)-dependent. Interacts with EZH2; required to repress RAR signaling
Subcellular location: Nucleus (Probable). Cell membrane
Miscellaneous: Tumor antigen recognized by cytolytic T lymphocytes
Secondary accessions: B2R6Y7 O43481 Q8IXN8

Explore the universe of human proteins at neXtProt for PRAME: NX_P78395

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P78395

  • PRAME Protein expression data from MOPED and PaxDb:    About this image 
    PRAME Protein Expression
    REFSEQ proteins (5 alternative transcripts): 
    NP_006106.1  NP_996836.1  NP_996837.1  NP_996838.1  NP_996839.1  

    ENSEMBL proteins: 
     ENSP00000381728   ENSP00000384343   ENSP00000385198   ENSP00000407320   ENSP00000407121  
     ENSP00000412318   ENSP00000384058   ENSP00000399816   ENSP00000385091   ENSP00000445675  
     ENSP00000381726   ENSP00000445097   ENSP00000407342  

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    Uscn Proteins for PRAME

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IEA--
    GO:0005886plasma membrane IEA--

    PRAME 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

    PRAME for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR026292 PRAME/Leu_rich_rep-con_p14
     IPR026271 PRAME_family

    Graphical View of Domain Structure for InterPro Entry P78395

    ProtoNet protein and cluster: P78395

    1 Blocks protein family: IPB001611 Leucine-rich repeat signature

    UniProtKB/Swiss-Prot: PRAME_HUMAN, P78395
    Similarity: Belongs to the PRAME family
    Similarity: Contains 4 LRR (leucine-rich) repeats


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: PRAME_HUMAN, P78395
    Function: Functions as a transcriptional repressor, inhibiting the signaling of retinoic acid through the retinoic acid
    receptors RARA, RARB and RARG. Prevents retinoic acid-induced cell proliferation arrest, differentiation and apoptosis

         Genatlas biochemistry entry for PRAME:
    preferentially expressed antigen in melanoma

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding IPI16179254
    GO:0042974retinoic acid receptor binding IDA16179254
         
    PRAME for ontologies           About GeneDecksing


    Animal Models:
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    miRNA
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    SwitchGear 3'UTR luciferase reporter plasmidPRAME 3' UTR sequence
    Inhib. RNA
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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 PRAME

    5/7 Interacting proteins for PRAME (P783951, 2, 3) via UniProtKB, MINT, STRING, and/or I2D (see all 7)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    STK19P498421, 2, 3EBI-348325,EBI-347581 MINT-62760 MINT-62684 MINT-62586 I2D: score=5 
    CUL2Q136172MINT-8295466 MINT-8295524 MINT-8295568 MINT-8295435 MINT-8295501 MINT-8295600 MINT-8295545
    TCEB1Q153692MINT-8295466 MINT-8295568 MINT-8295435 MINT-8295501 MINT-8295600 MINT-8295545
    TCEB2Q153702MINT-8295466 MINT-8295568 MINT-8295435 MINT-8295545
    NEDD8Q158432MINT-8295466 MINT-8295524 MINT-8295501
    About this table

    Gene Ontology (GO): 5/9 biological process terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--
    GO:0006915apoptotic process IEA--
    GO:0008284positive regulation of cell proliferation IDA16179254
    GO:0030154cell differentiation IEA--
    GO:0040008regulation of growth IEA--

    PRAME 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
    Browse drugs & compounds from Enzo Life Sciences

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

    (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, Sirion Biotech, 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 PRAME gene (5 alternative transcripts): 
    NM_006115.3  NM_206953.1  NM_206954.1  NM_206955.1  NM_206956.1  

    Unigene Cluster for PRAME:

    Preferentially expressed antigen in melanoma
    Hs.30743  [show with all ESTs]
    Unigene Representative Sequence: BC022008
    16 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000398743(uc002zwf.3 uc010gtr.3 uc002zwi.3 uc002zwj.3)
    ENST00000492657(uc002zwk.3) ENST00000405655 ENST00000402697 ENST00000439106
    ENST00000438888 ENST00000420709 ENST00000476336 ENST00000485532 ENST00000406503
    ENST00000442481 ENST00000403441 ENST00000543184 ENST00000398741(uc002zwg.3 uc002zwh.3)
    ENST00000539862(uc011air.2) ENST00000424204

    miRNA
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    Inhib. RNA
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat PRAME

    Additional cDNA sequence: 

    AF025440.1 AK129783.1 AK302188.1 AK304593.1 AK312769.1 AK316395.1 BC014074.2 BC022008.1 
    BC039731.1 CR456549.1 U65011.1 

    19 DOTS entries:

    DT.314248  DT.97783168  DT.101964572  DT.40131245  DT.92444168  DT.92444174  DT.100757437  DT.97851491 
    DT.100825285  DT.100825299  DT.120677185  DT.92444178  DT.100825292  DT.91805738  DT.100825297  DT.120677343 
    DT.120677810  DT.120676911  DT.100825293 

    24/330 AceView cDNA sequences (see all 330):

    NM_206954 BM473529 BE893611 AA861253 BX371299 CR604772 BG035204 BG769045 
    AA496991 BQ439970 CD244596 BQ219052 CR456549 BQ070867 BQ230496 AW169285 
    BE891938 BE408826 AI744982 CR611321 BI825495 BE302526 BE898376 BU171925 

    GeneLoc Exon Structure

    5/8 Alternative Splicing Database (ASD) splice patterns (SP) for PRAME (see all 8)    About this scheme

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


    ECgene alternative splicing isoforms for PRAME

    (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

    PRAME expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TAGGAGTTAA
    PRAME Expression
    About this image
    See PRAME Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for PRAME

    SOURCE GeneReport for Unigene cluster: Hs.30743

    UniProtKB/Swiss-Prot: PRAME_HUMAN, P78395
    Tissue specificity: Expressed in testis. Detected in samples of kidney, brain and skin

        SABiosciences Custom PCR Arrays for PRAME
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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 PRAME (if available)
    TreeFam Gene Tree for PRAME (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for PRAME gene
    PRAMEF192  PRAMEF102  PRAMEF32  PRAMEF202  LOC6453592  PRAMEF182  PRAMEF122  PRAMEF212  
    PRAMEF152  PRAMEF222  PRAMEF42  PRAMEF22  PRAMEF132  PRAMEF92  LRRC14B2  PRAMEF142  
    PRAMEF72  PRAMEF82  PRAMEF172  LRRC142  PRAMEF52  PRAMEF112  PRAMEF162  PRAMEF12  
    PRAMEF62  
    18/26 SIMAP similar genes for PRAME using alignment to 8 protein entries:     PRAME_HUMAN (see all proteins) (see all similar genes):
    PRAMEF12    PRAMEF24    PRAMEF7    PRAMEF8    LOC645359    PRAMEF15
    PRAMEF9    PRAMEF19    PRAMEF20    PRAMEF21    PRAMEF23    PRAMEF4
    PRAMEF5    PRAMEF6    PRAMEF11    PRAMEF25    PRAMEF3    PRAMEF10

    PRAME 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

    10/80 NCBI SNPs in PRAME are shown (see all 80    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 22 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs136041,2
    C,F,O,H--22890492(-) CCTAAC/TTAGCT 10 N syn1 ese320Minor allele frequency- T:0.11MN NA NS EA WA EU 8149
    rs2002621671,2
    --22890536(+) ATAGAA/CGGTTC 10 V F mis10--------
    rs617308401,2
    C,F--22890552(+) CCACAG/ATGAGG 10 /H syn14Minor allele frequency- A:0.00NS NA EU 6069
    rs2019650171,2
    --22890562(+) GACAGC/GGGTTG 10 P R mis10--------
    rs2014765431,2
    --22890593(+) GGGCCA/GCCCCA 10 R W mis10--------
    rs2001829631,2
    --22890632(+) ATGCAC/GATAGG 10 L V mis10--------
    rs1454609931,2
    C,F--22890642(+) GCAAGC/ACTCTC 10 /R /S mis11Minor allele frequency- A:0.00NA 4548
    rs1472811701,2
    C--22890704(+) CAGCAC/GGTGGG 10 L V mis11Minor allele frequency- G:0.00NA 4552
    rs57587021,2
    H--22890713(+) GGTCAG/CATTGC 10 /L /V mis14Minor allele frequency- C:0.00NS EA 400
    rs1407913021,2
    C,F--22890715(+) TCAGAT/CTGCTC 10 /N /S mis11Minor allele frequency- C:0.00NA 4552

    HapMap Linkage Disequilibrium report for PRAME (22890123 - 22901768 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 35 variations for PRAME
         15/35 CNVs (see all 35): 90933 59061 34540 90934 5356 35989 9835 5175 90937 0334 35987 35996 53720 2019 90936

    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, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    PRAME for disorders           About GeneDecksing

    OMIM gene information: 606021    OMIM disorders: --

    20/36 diseases for PRAME (see all 36):    About MalaCards
    melanoma    acute leukemia    leukemia    diffuse large b-cell lymphoma
    b-cell lymphomas    testicular germ cell tumor    soft tissue sarcoma    germ cell tumor
    myeloid leukemia    hairy cell leukemia    mantle cell lymphoma    lymphoblastic leukemia
    cervical squamous cell carcinoma    acute promyelocytic leukemia    squamous cell carcinoma    acute lymphoblastic leukemia
    chronic lymphocytic leukemia    acute myeloid leukemia    chronic myeloid leukemia    lymphocytic leukemia

    1 disease from the University of Copenhagen DISEASES database for PRAME:
    Leukemia

    10/14 Novoseek disease relationships for PRAME gene (see all 14)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    minimal residual disease 72.5 11 18950857 (2), 11298586 (2), 11943337 (1), 16860864 (1) (see all 7)
    melanoma 60.5 24 9753074 (2), 16707612 (2), 10682862 (2), 16179254 (1) (see all 14)
    blast crisis 53.9 3 17157168 (1), 17382387 (1)
    acute leukemia 53.8 7 16860864 (3), 16044453 (2), 9753074 (1), 12620290 (1)
    myeloid leukemia chronic 52.6 3 17382387 (2), 10682862 (1)
    leukemia 45.1 11 16978861 (2), 11298586 (2), 16681423 (2), 16044453 (1) (see all 8)
    solid tumor 36 3 16044453 (1), 16860864 (1), 18295331 (1)
    tumors 34.3 20 15240516 (3), 18709641 (3), 16044453 (2), 12419593 (2) (see all 11)
    lymphoblastic leukemia acute 27.7 1 12419593 (1)
    cancer 26.1 11 9740504 (2), 10741395 (2), 12620290 (1), 16179254 (1) (see all 8)


    Export disorders for PRAME 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 PRAME gene, integrated from 9 sources (see all 98):
    (articles sorted by number of sources associating them with PRAME)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Characterization of an antigen that is recognized on a melanoma showing partial HLA loss by CTL expressing an NK inhibitory receptor. (PubMed id 9047241)1, 2, 3, 9 Ikeda H.... Coulie P.G. (1997)
    2. The human tumor antigen PRAME is a dominant repressor of retinoic acid receptor signaling. (PubMed id 16179254)1, 2, 9 Epping M.T....Bernards R. (2005)
    3. PRAME is a membrane and cytoplasmic protein aberrantly expressed in chronic lymphocytic leukemia and mantle cell lymphoma. (PubMed id 16620968)1, 2 Proto-Siqueira R.... Zago M.A. (2006)
    4. A genome annotation-driven approach to cloning the human ORFeome. (PubMed id 15461802)1, 2 Collins J.E.... Dunham I. (2004)
    5. 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)
    6. The DNA sequence of human chromosome 22. (PubMed id 10591208)1, 3 Dunham I....O'Brien K.P. (1999)
    7. Using the yeast two-hybrid system to identify human epithelial cell proteins that bind gonococcal Opa proteins: intracellular gonococci bind pyruvate kinase via their Opa proteins and require host pyruvate for growth. (PubMed id 9466265)1, 2 Williams J.M.... Rest R.F. (1998)
    8. Aberrant hypomethylation of the cancer-testis antigen PRAME correlates with PRAME expression in acute myeloid leukemia. (PubMed id 18587578)1, 9 Ortmann C.A....Zeschnigk M. (2008)
    9. Epigenetic regulation of PRAME gene in chronic myeloid leukemia. (PubMed id 17382387)1, 9 Roman-Gomez J....Torres A. (2007)
    10. Expression patterns of WT1 and PRAME in acute myeloid leukemia patients and their usefulness for monitoring minimal residual disease. (PubMed id 18950857)1, 9 Qin Y....Huang X. (2009)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 23532 HGNC: 9336 AceView: PRAME Ensembl:ENSG00000185686 euGenes: HUgn23532
    ECgene: PRAME H-InvDB: PRAME

    (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 PRAME Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for PRAME 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 PRAME gene:
    Search GeneIP for patents involving PRAME

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



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