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

HNRNPH3 Gene

protein-coding   GIFtS: 54
GCID: GC10P070090

Heterogeneous Nuclear Ribonucleoprotein H3 (2H9)


(Previous symbol: HNRPH3)
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(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
Heterogeneous Nuclear Ribonucleoprotein H3 (2H9)1 2     HnRNP H32 3
HNRPH31 2 3 5     2H92 5
Heterogeneous Nuclear Ribonucleoprotein 2H92 3     Heterogeneous Nuclear Ribonucleoprotein H32
HnRNP 2H92 3     

External Ids:    HGNC: 50431   Entrez Gene: 31892   Ensembl: ENSG000000967467   OMIM: 6023245   UniProtKB: P319423   

Export aliases for HNRNPH3 gene to outside databases

Previous GC identifers: GC10P069762 GC10P064093


(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 HNRNPH3 Gene:
This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs).
The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are
associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA
metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the
nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded
by this gene has two repeats of quasi-RRM domains that bind to RNAs. It is localized in nuclear bodies of the
nucleus. This protein is involved in the splicing process and it also participates in early heat shock-induced
splicing arrest by transiently leaving the hnRNP complexes. Several alternatively spliced transcript variants
have been noted for this gene, however, not all are fully characterized. (provided by RefSeq, Jul 2008)

GeneCards Summary for HNRNPH3 Gene: 
HNRNPH3 (heterogeneous nuclear ribonucleoprotein H3 (2H9)) is a protein-coding gene. Diseases associated with HNRNPH3 include reticulosarcoma, and anterior uveitis. GO annotations related to this gene include RNA binding and nucleotide binding. An important paralog of this gene is RBM12B.

UniProtKB/Swiss-Prot: HNRH3_HUMAN, P31942
Function: Involved in the splicing process and participates in early heat shock-induced splicing arrest. Due to
their great structural variations the different isoforms may possess different functions in the splicing reaction

Gene Wiki entry for HNRNPH3 (HNRPH3) 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_000010.10  NT_030059.13  NC_018921.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HNRNPH3 gene promoter:
         Pbx1a   AML1a   Pax-2   Evi-1   NF-AT   MZF-1   NF-AT4   NF-AT2   NF-AT3   NF-AT1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidHNRNPH3 promoter sequence
   Search SABiosciences Chromatin IP Primers for HNRNPH3

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat HNRNPH3


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

Entrez Gene cytogenetic band: 10q22   Ensembl cytogenetic band:  10q21.3   HGNC cytogenetic band: 10q22

HNRNPH3 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
HNRNPH3 gene location

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10P070090:  view genomic region     (about GC identifiers)

Start:
70,090,931 bp from pter      End:
70,102,953 bp from pter
Size:
12,023 bases      Orientation:
plus 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: HNRH3_HUMAN, P31942 (See protein sequence)
Recommended Name: Heterogeneous nuclear ribonucleoprotein H3  
Size: 346 amino acids; 36926 Da
Subcellular location: Nucleus
Secondary accessions: A8K682 B3KRE1 Q9BSX1 Q9NP53 Q9NP96 Q9NPA7 Q9NPI4 Q9UFU4 Q9Y4J5
Alternative splicing: 6 isoforms:  P31942-1   P31942-2   P31942-3   P31942-4   P31942-5   P31942-6   

Explore the universe of human proteins at neXtProt for HNRNPH3: NX_P31942

Explore proteomics data for HNRNPH3 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_P31942

  • HNRNPH3 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    HNRNPH3 Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_036339.1  NP_067676.2  

    ENSEMBL proteins: 
     ENSP00000265866   ENSP00000346726   ENSP00000409869  

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    Browse Proteins at Cloud-Clone Corp. 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0030529ribonucleoprotein complex IEA--

    HNRNPH3 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
    HGNC Gene Families: 
    RBM: RNA binding motif (RRM) containing

    2 InterPro protein domains:
     IPR012677 Nucleotide-bd_a/b_plait
     IPR000504 RRM_dom

    Graphical View of Domain Structure for InterPro Entry P31942

    ProtoNet protein and cluster: P31942

    1 Blocks protein domain: IPB000504 RNA-binding region RNP-1 (RNA recognition motif)

    UniProtKB/Swiss-Prot: HNRH3_HUMAN, P31942
    Similarity: Contains 2 RRM (RNA recognition motif) domains


    HNRNPH3 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: HNRH3_HUMAN, P31942
    Function: Involved in the splicing process and participates in early heat shock-induced splicing arrest. Due to
    their great structural variations the different isoforms may possess different functions in the splicing reaction

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000166nucleotide binding IEA--
    GO:0003676nucleic acid binding ----
    GO:0003723RNA binding NAS10858537
         
    HNRNPH3 for ontologies           About GeneDecksing


    Phenotypes:
         2 GenomeRNAi human phenotypes for HNRNPH3:
     Increased G1 DNA content  Synthetic lethal with c-Myc af 

    Animal Models:
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    SwitchGear 3'UTR luciferase reporter plasmidHNRNPH3 3' UTR sequence
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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:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for HNRNPH3

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/107 Interacting proteins for HNRNPH3 (P319422, 3 ENSP000002658664) via UniProtKB, MINT, STRING, and/or I2D (see all 107)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    RPS4XP627012, 3, ENSP000003627444MINT-63658 I2D: score=4 STRING: ENSP00000362744
    ZMYM2Q9UBW72, 3, ENSP000003723224MINT-62318 I2D: score=3 STRING: ENSP00000372322
    C14orf1Q9UKR52, 3MINT-63665 I2D: score=5 
    CRMP1Q141942, 3MINT-63659 I2D: score=5 
    EEF1GP266412, 3MINT-63657 I2D: score=5 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000398mRNA splicing, via spliceosome NAS10858537
    GO:0006396RNA processing TAS8999868
    GO:0008380RNA splicing TAS8999868

    HNRNPH3 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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for HNRNPH3 (HNRH3)

    Search CenterWatch for drugs/clinical trials and news about HNRNPH3 / HNRH3

    (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 HNRNPH3 gene (2 alternative transcripts): 
    NM_012207.2  NM_021644.3  

    Unigene Cluster for HNRNPH3:

    Heterogeneous nuclear ribonucleoprotein H3 (2H9)
    Hs.643472  [show with all ESTs]
    Unigene Representative Sequence: NM_012207
    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000469172(uc009xpu.3) ENST00000461310 ENST00000265866(uc001jnw.4 uc001jnx.4 uc010qiv.2)
    ENST00000480987 ENST00000486854 ENST00000467249 ENST00000354695 ENST00000481819
    ENST00000491200(uc001jny.4) ENST00000490442 ENST00000478698 ENST00000441000


    miRNA
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    hsa-miR-194* hsa-miR-140-5p hsa-miR-142-5p hsa-miR-411 hsa-miR-340 hsa-miR-548l hsa-miR-570 hsa-miR-7-1*
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    Additional mRNA sequence: 

    AF052131.1 AF132361.1 AF132362.1 AK223441.1 AK291547.1 AK295316.1 BC004511.2 BC039824.1 

    24/40 DOTS entries (see all 40):

    DT.97814563  DT.448460  DT.97780489  DT.102836965  DT.95267874  DT.91755504  DT.100044954  DT.100655854 
    DT.95267871  DT.100674048  DT.100044957  DT.100044959  DT.100858854  DT.121257648  DT.100674045  DT.95267904 
    DT.100674046  DT.121257676  DT.100809833  DT.100674043  DT.91696639  DT.95233774  DT.97779866  DT.95191783 

    24/395 AceView cDNA sequences (see all 395):

    BM727025 AA328756 CB116933 AF132364 C03134 AA417077 BE254298 AF052131 
    AV681827 CF272498 BU931630 CA417933 CD677991 AI591106 BM803843 BU742127 
    BQ223146 AI192388 BU145773 BU541342 AW189387 BM800363 CA407019 AA497024 

    GeneLoc Exon Structure

    5/23 Alternative Splicing Database (ASD) splice patterns (SP) for HNRNPH3 (see all 23)    About this scheme

    ExUns: 1 ^ 2a · 2b · 2c · 2d · 2e · 2f · 2g · 2h · 2i ^ 3 ^ 4a · 4b · 4c · 4d ^ 5a · 5b ^ 6 ^ 7a · 7b · 7c · 7d ^ 8a · 8b · 8c · 8d ·
    SP1:                                                        -     -     -           -     -     -           -                 -     -                           
    SP2:                                                                                                        -                 -     -                           
    SP3:                                                                                                                                                            
    SP4:                                                              -     -           -     -     -     -     -                 -     -                           
    SP5:                                                        -     -     -           -     -     -           -                       -                           

    ExUns: 8e ^ 9a · 9b · 9c · 9d ^ 10a · 10b ^ 11 ^ 12a · 12b ^ 13
    SP1:  -                                                               
    SP2:  -                                                               
    SP3:  -                                                               
    SP4:  -                                                               
    SP5:  -                                                               


    ECgene alternative splicing isoforms for HNRNPH3

    (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

    HNRNPH3 expression in normal human tissues (normalized intensities)      HNRNPH3 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: AGTGGAGGTG
    HNRNPH3 Expression
    About this image


    HNRNPH3 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/3 selected tissues (see all 3) fully expand
     
     Neural Tube (Nervous System)    fully expand to see all 2 entries
             Diencephalon
     
     Brain (Nervous System)    fully expand to see all 2 entries
             brain/midbrain   
     
     Thyroid (Endocrine System)

    See HNRNPH3 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for HNRNPH3

    SOURCE GeneReport for Unigene cluster: Hs.643472
        SABiosciences Custom PCR Arrays for HNRNPH3
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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

    This gene was present in the common ancestor of chordates.

    Orthologs for HNRNPH3 gene from 5/13 species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Hnrnph31 , 5 heterogeneous nuclear ribonucleoprotein H31, 5 94.86(n)1
    99.4(a)1
      10 (32.52 cM)5
    4324671  NM_001079824.11  NP_001073293.11 
     630146645 
    chicken
    (Gallus gallus)
    Aves HNRNPH31 heterogeneous nuclear ribonucleoprotein H3 (2H9) 86.07(n)
    92.57(a)
      423686  NM_001012592.1  NP_001012610.1 
    lizard
    (Anolis carolinensis)
    Reptilia HNRNPH36
    Uncharacterized protein
    92(a)
    1 ↔ 1
    GL343215.1(1485372-1492946)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.52362 Xenopus laevis transcribed sequence with moderate similarity more 80.12(n)    CD302920.1 
    zebrafish
    (Danio rerio)
    Actinopterygii HNRNPH36
    heterogeneous nuclear ribonucleoprotein H3 (2H9)
    51(a)
    1 ↔ 1
    13(23003728-23012629)


    ENSEMBL Gene Tree for HNRNPH3 (if available)
    TreeFam Gene Tree for HNRNPH3 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HNRNPH3 gene
    RBM12B2  ESRP12  HNRNPH22  GRSF12  ESRP22  HNRNPH12  HNRNPF2  RBM122  
    6 SIMAP similar genes for HNRNPH3 using alignment to 2 protein entries:     HNRH3_HUMAN (see all proteins):
    HNRNPH1    DKFZp686A15170    GRSF1    HNRNPH2    OK/SW-cl.23    HNRNPF

    HNRNPH3 for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for HNRNPH3
    PGOHUM00000241869


    (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

    10/171 SNPs in HNRNPH3 are shown (see all 171)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1880257911,2
    --70094726(+) GGTAGA/GGTGAG 2 -- int10--------
    rs1141734781,2
    F--70094772(+) ACCCTA/GTAAAA 2 -- int11Minor allele frequency- G:0.10WA 118
    rs1163386141,2
    C--70094778(+) TAAAAC/TAGATT 2 -- int10--------
    rs1420663051,2
    --70094812(+) TTTCCA/GCAATT 2 -- int10--------
    rs341334191,2
    C--70094868(+) AACAC-/TTTTTT 2 -- int10--------
    rs764854971,2
    --70094992(+) CTTTTC/TTTTTT 2 -- int10--------
    rs724088221,2
    C--70094993(+) TTTTC-/TTTTTTT 2 -- int10--------
    rs1925343041,2
    --70095088(+) CTTCAA/GTTTTT 2 -- int10--------
    rs782601981,2
    C--70095195(+) AAAAAA/TAAATA 2 -- int10--------
    rs2007546151,2
    --70095197(+) AAATA-/AATAAAAC 2 -- int10--------

    HapMap Linkage Disequilibrium report for HNRNPH3 (70090931 - 70102953 bp)

    Structural Variations
          Database of Genomic Variants (DGV) variations for HNRNPH3: --

    Human Gene Mutation Database (HGMD): HNRNPH3
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing HNRNPH3
    DNA2.0 Custom Variant and Variant Library Synthesis for HNRNPH3

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 602324    OMIM disorders: --

    9 diseases for HNRNPH3:    About MalaCards
    reticulosarcoma    anterior uveitis    malignant histiocytosis    histiocytosis
    uveitis    neuroblastoma    alzheimer's disease    hepatocellular carcinoma
    endotheliitis


    HNRNPH3 for disorders           About GeneDecksing


    Congresses - knowledge worth sharing:  
    Alzheimer's & Parkinson's Diseases Congress (ADPD) 18 - 22 March 2015
    Genetic Association Database (GAD): HNRNPH3
    Human Genome Epidemiology (HuGE) Navigator: HNRNPH3 (1 document)

    Export disorders for HNRNPH3 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 HNRNPH3 gene, integrated from 9 sources (see all 63):
    (articles sorted by number of sources associating them with HNRNPH3)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Cloning of human 2H9 heterogeneous nuclear ribonucleoproteins. Relation with splicing and early heat shock-induced splicing arrest. (PubMed id 8999868)1, 2, 3, 9 Mahe D....Fuchs J.-P. (1997)
    2. The hnRNP 2H9 gene, which is involved in the splicing reaction, is a multiply spliced gene. (PubMed id 10858537)1, 2, 9 Honore B. (2000)
    3. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. (PubMed id 16385451)1, 4 Grupe A....Goate A. (2006)
    4. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1, 2 Olsen J.V....Mann M. (2006)
    5. Immunoaffinity profiling of tyrosine phosphorylation in cancer cells. (PubMed id 15592455)1, 2 Rush J.... Comb M.J. (2005)
    6. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    7. 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)
    8. A post-translational modification of nuclear proteins, N(G),N(G)- dimethyl-Arg, found in a natural HLA class I peptide ligand. (PubMed id 11152131)1, 2 Yague J.... Lopez de Castro J.A. (2000)
    9. Microsequences of 145 proteins recorded in the two-dimensional gel protein database of normal human epidermal keratinocytes. (PubMed id 1286667)1, 2 Rasmussen H.H....Vandekerckhove J. (1992)
    10. VCP phosphorylation-dependent interaction partners pre vent apoptosis in Helicobacter pylori-infected gastric epithelial cells. (PubMed id 23383273)1 Yu C.C....Chow L.P. (2013)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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      Query String
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      (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: 3189 HGNC: 5043 AceView: HNRPH3 Ensembl:ENSG00000096746 euGenes: HUgn3189
    ECgene: HNRNPH3 H-InvDB: HNRNPH3

    (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 HNRNPH3 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 HNRNPH3 gene:
    Search GeneIP for patents involving HNRNPH3

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



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