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

HNRNPF Gene

protein-coding   GIFtS: 56
GCID: GC10M043881

heterogeneous nuclear ribonucleoprotein F


(Previous symbol: HNRPF)
 Explore 14 diseases affiliated with
HNRNPF via our new
 Human Malady Compendium 
Biological research products
for HNRNPF
    

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

Aliases
Heterogeneous Nuclear Ribonucleoprotein F1 2     HnRNP F Protein2
HNRPF1 2 3 5     Mcs94-11
Nucleolin-Like Protein Mcs94-12 3     HnRNP F3
OK/SW-Cl.231     

External Ids:    HGNC: 50391   Entrez Gene: 31852   Ensembl: ENSG000001698137   OMIM: 6010375   UniProtKB: P525973   

Export aliases for HNRNPF gene to outside databases

Previous GC identifers: GC10M043202 GC10M040407


(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 HNRNPF:
This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The
hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated
with pre-mRNAs in the nucleus and regulate alternative splicing, polyadenylation, 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
three repeats of quasi-RRM domains that bind to RNAs which have guanosine-rich sequences. This protein is very similar
to the family member hnRPH. Multiple alternatively spliced variants, encoding the same protein, have been identified.
(provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: HNRPF_HUMAN, P52597
Function: Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for
the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Plays a
role in the regulation of alternative splicing events. Binds G-rich sequences in pre-mRNAs and keeps target RNA in an
unfolded state

Gene Wiki entry for HNRNPF (HNRPF)


(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_000010.10  NC_018921.1  NT_033985.7  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HNRNPF gene promoter:
         Elk-1   Meis-1   c-Ets-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidHNRNPF promoter sequence
   Search SABiosciences Chromatin IP Primers for HNRNPF

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


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

Entrez Gene cytogenetic band: 10q11.21   Ensembl cytogenetic band:  10q11.21   HGNC cytogenetic band: 10q11.21

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

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10M043881:  view genomic region     (about GC identifiers)

Start:
43,881,065 bp from pter      End:
43,904,696 bp from pter
Size:
23,632 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: HNRPF_HUMAN, P52597 (See protein sequence)
Recommended Name: Heterogeneous nuclear ribonucleoprotein F  
Size: 415 amino acids; 45672 Da
Subunit: Identified in the spliceosome C complex. Interacts with EIF2C1, EIF2C2, TBP and TXNL4/DIM1
Subcellular location: Nucleus, nucleoplasm
6/7 PDB 3D structures from and Proteopedia for HNRNPF (see all 7):
2HGL (3D)        2HGM (3D)        2HGN (3D)        2KFY (3D)        2KG0 (3D)        2KG1 (3D)    
Secondary accessions: B3KM84 Q5T0N2 Q96AU2

Explore the universe of human proteins at neXtProt for HNRNPF: NX_P52597

Post-translational modifications:

  • Sumoylated1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P52597

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

    REFSEQ proteins (6 alternative transcripts): 
    NP_001091674.1  NP_001091675.1  NP_001091676.1  NP_001091677.1  NP_001091678.1  NP_004957.1  

    ENSEMBL proteins: 
     ENSP00000349573   ENSP00000348345   ENSP00000338477   ENSP00000438061   ENSP00000400433  
    Reactome Protein details: P52597
    Human Recombinant Protein Products: 
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    Uscn Proteins for HNRNPF

    Gene Ontology (GO): 5/7 cellular component terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005654nucleoplasm TAS--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm IDA--
    GO:0030529ribonucleoprotein complex ----


    HNRNPF for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for HNRNPF


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

    HNRNPF for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR012996 Znf_CHHC
     IPR012677 Nucleotide-bd_a/b_plait
     IPR000504 RRM_dom

    Graphical View of Domain Structure for InterPro Entry P52597

    ProtoNet protein and cluster: P52597

    2 Blocks protein families:
    IPB000504 RNA-binding region RNP-1 (RNA recognition motif)
    IPB012996 Zinc finger


    UniProtKB/Swiss-Prot: HNRPF_HUMAN, P52597
    Domain: The N-terminal RRM domains are responsible for recognizing the G-tract of BCL-X RNA
    Similarity: Contains 3 RRM (RNA recognition motif) domains


    (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: HNRPF_HUMAN, P52597
    Function: Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for
    the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Plays a
    role in the regulation of alternative splicing events. Binds G-rich sequences in pre-mRNAs and keeps target RNA in an
    unfolded state

    miRNA
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    hsa-miR-124* hsa-miR-3685 hsa-miR-3146 hsa-miR-128 hsa-miR-139-5p hsa-miR-29a hsa-miR-200a hsa-miR-16-1*
    SwitchGear 3'UTR luciferase reporter plasmidHNRNPF 3' UTR sequence
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    Gene Ontology (GO): 5 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 TAS7499401
    GO:0003727single-stranded RNA binding IDA--
    GO:0005515protein binding IPI17932509


    HNRNPF for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for HNRNPF:
     Decreased p24 protein expressi 


    (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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1mRNA Splicing - Major Pathway
    mRNA Splicing1.00
    Processing of Capped Intron-Containing Pre-mRNA0.96
    mRNA Splicing - Major Pathway1.00
    mRNA Processing0.82
    2Generic Transcription Pathway
    Gene Expression0.46

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    5        Reactome Pathways for HNRNPF
        mRNA Splicing - Major Pathway
    mRNA Splicing
    Gene Expression
    mRNA Processing
    Processing of Capped Intron-Containing Pre-mRNA



    HNRNPF for pathways           About GeneDecksing

    Interactions:

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

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

    5/965 Interacting proteins for HNRNPF (P525972, 3 ENSP000003384774) via UniProtKB, MINT, STRING, and/or I2D (see all 965)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    HNRNPH1P319432, 3, ENSP000003491684MINT-7945693 MINT-7947479 I2D: score=3 STRING: ENSP00000349168
    NSFP464592, 3MINT-7945693 MINT-7947479 I2D: score=1 
    SRRM2Q9UQ352, 3, ENSP000003017404MINT-7945693 I2D: score=1 STRING: ENSP00000301740
    UBA5Q9GZZ92, 3MINT-7945693 MINT-7947479 I2D: score=1 
    PRPF40AO754002, 3MINT-7945693 I2D: score=2 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000398mRNA splicing, via spliceosome TAS--
    GO:0006396RNA processing TAS7499401
    GO:0008380RNA splicing TAS--
    GO:0010467gene expression TAS--
    GO:0043484regulation of RNA splicing IMP9111328


    HNRNPF 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 HNRNPF
    Search CenterWatch for drugs/clinical trials and news about HNRNPF / HNRPF 

    (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,
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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 HNRNPF gene (6 alternative transcripts): 
    NM_001098204.1  NM_001098205.1  NM_001098206.1  NM_001098207.1  NM_001098208.1  NM_004966.3  

    Unigene Cluster for HNRNPF:

    Heterogeneous nuclear ribonucleoprotein F
    Hs.808  [show with all ESTs]
    Unigene Representative Sequence: NM_001098208
    7 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000357065(uc001jas.2 uc001jav.2 uc001jau.2) ENST00000356053(uc001jat.2)
    ENST00000337970 ENST00000477108 ENST00000498176 ENST00000544000(uc001jar.2)
    ENST00000443950(uc009xmh.1)

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    8/55 QIAGEN miScript miRNA Assays for microRNAs that regulate HNRNPF (see all 55):
    hsa-miR-124* hsa-miR-3685 hsa-miR-3146 hsa-miR-128 hsa-miR-139-5p hsa-miR-29a hsa-miR-200a hsa-miR-16-1*
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    Inhib. RNA
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    Additional cDNA sequence: 

    AB062287.1 AK001364.1 AK296696.1 BC001432.2 BC004254.1 BC015580.2 BC016736.1 BC106008.1 
    L28010.1 

    24/48 DOTS entries (see all 48):

    DT.92463968  DT.95341421  DT.99991983  DT.86855111  DT.100038746  DT.95341433  DT.100038744  DT.101973798 
    DT.100643538  DT.100639461  DT.100657795  DT.92463949  DT.100639456  DT.92463969  DT.121237919  DT.121237926 
    DT.95341435  DT.95341331  DT.121237788  DT.95341422  DT.121237829  DT.100686078  DT.100657802  DT.100657798 

    24/902 AceView cDNA sequences (see all 902):

    BG675947 BQ876653 BE889737 BM768105 AV708126 BM770598 BM759015 CA308134 
    AI678404 BC001432 BQ220363 BI756772 CD368610 BC004254 CA773672 BM982395 
    BM717481 BQ437331 CR608803 BM541978 BF528122 AL541901 BM826622 BG387546 

    GeneLoc Exon Structure

    5/20 Alternative Splicing Database (ASD) splice patterns (SP) for HNRNPF (see all 20)    About this scheme

    ExUns: 1a · 1b · 1c · 1d · 1e ^ 2a · 2b ^ 3a · 3b · 3c ^ 4a · 4b · 4c ^ 5a · 5b · 5c ^ 6a · 6b ^ 7a · 7b ^ 8 ^ 9a · 9b ^ 10a · 10b · 10c ·
    SP1:                          -     -     -     -     -     -     -     -     -     -     -     -     -           -     -                                       
    SP2:                          -     -     -     -     -     -     -     -     -     -     -           -           -     -           -     -                     
    SP3:                                                                                -     -     -     -           -     -                                       
    SP4:                                                                                                  -           -     -           -     -                     
    SP5:                          -     -     -     -     -     -     -     -     -     -     -     -     -           -     -           -     -                     

    ExUns: 10d · 10e · 10f · 10g · 10h · 10i · 10j · 10k · 10l · 10m · 10n
    SP1:                                                                  
    SP2:                                                                  
    SP3:                                                                  
    SP4:                                                                  
    SP5:                                                                  


    ECgene alternative splicing isoforms for HNRNPF

    (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

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

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

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

    SOURCE GeneReport for Unigene cluster: Hs.808

    UniProtKB/Swiss-Prot: HNRPF_HUMAN, P52597
    Tissue specificity: Expressed ubiquitously

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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 eukaryotes.

    Orthologs for HNRNPF gene from 4/17 species (see all 17)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    fruit fly
    (Drosophila melanogaster)
    Insecta glo6
    glorund
    23(a)
    1 → many
    3R(7640928-7645142)
    worm
    (Caenorhabditis elegans)
    Secernentea hrpf-11 Protein HRPF-1 43.85(n)
    37.46(a)
      172395  NM_170888.3  NP_740877.1 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT5G660106
    AT3G208906
    RNA-binding (RRM/RBD/RNP motifs) family protein
    33(a)
    27(a)
    many ↔ many
    many ↔ many
    5(26399432-26400999)
    3(7319848-7321054)
    rice
    (Oryza sativa)
    Liliopsida --
    --
    RNA recognition motif containing protein, putative...
    RNA recognition motif containing protein, putative...
    31(a)
    30(a)
    many ↔ many
    many ↔ many
    12(1496364-1498413)
    11(1550980-1553325)


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HNRNPF gene
    RBM12B2  HNRNPH32  HNRNPH22  ESRP12  GRSF12  HNRNPH12  ESRP22  RBM122  
    5 SIMAP similar genes for HNRNPF using alignment to 1 protein entry:     HNRPF_HUMAN:
    DKFZp686A15170    HNRNPH1    HNRNPH2    HNRNPH3    GRSF1

    HNRNPF for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for HNRNPF
    PGOHUM00000250544


    (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

    10/472 NCBI SNPs in HNRNPF are shown (see all 472    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs741357401,2
    C,--43880592(+) TGGAAC/GGAAGG 6 -- ds50012Minor allele frequency- G:0.04WA 120
    rs1505191941,2
    --43880593(+) GGAACA/GAAGGG 6 -- ds50010--------
    rs1846935061,2
    --43880614(+) GGTGAA/GCCTCT 6 -- ds50010--------
    rs727852561,2
    C,F,--43880649(+) CTGAAG/AACTTC 6 -- ds50012Minor allele frequency- A:0.12WA NA 238
    rs1903733331,2
    --43880666(+) CTAATA/TTTTAA 6 -- ds50010--------
    rs749345041,2
    C,--43880800(+) TTGAA-/GAATTCCC 6 -- ds50010--------
    rs1822080041,2
    --43880816(+) AATGGC/TAGATA 6 -- ds50010--------
    rs79205391,2
    C,F,A,H,--43880833(+) TTGCAT/CAGAAT 6 -- ds500134Minor allele frequency- C:0.47NA NS EA WA CSA 3332
    rs1152963601,2
    F,--43880837(+) ACAGAA/GTGGTT 6 -- ds50011Minor allele frequency- G:0.03WA 118
    rs1855879031,2
    --43880996(+) GCTTGA/TTAATG 6 -- ds50010--------

    HapMap Linkage Disequilibrium report for HNRNPF (43881065 - 43904696 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for HNRNPF
         1 Indel: 60010

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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

    HNRNPF for disorders           About GeneDecksing

    OMIM gene information: 601037    OMIM disorders: --

    14 diseases for HNRNPF:    About MalaCards
    sipple syndrome    gout    endometrial cancer    colon carcinoma
    hepatocellular carcinoma    alzheimer's disease    colon cancer    prostate cancer
    ataxia    carcinoma    prostatitis    neuronitis
    pancreatic cancer    pancreatitis

    Human Genome Epidemiology (HuGE) Navigator: HNRNPF (2 documents)

    Export disorders for HNRNPF 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 HNRNPF gene, integrated from 9 sources (see all 94):
    (articles sorted by number of sources associating them with HNRNPF)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Heterogeneous nuclear ribonucleoproteins H, H', and F are members of a ubiquitously expressed subfamily of related but distinct proteins encoded by genes mapping to different chromosomes. (PubMed id 7499401)1, 2, 3 Honore B.... Celis J.E. (1995)
    2. Structural basis of G-tract recognition and encaging by hnRNP F quasi-RRMs. (PubMed id 20526337)1, 2 Dominguez C....Allain F.H. (2010)
    3. Proteomic and functional analysis of Argonaute-containing mRNA- protein complexes in human cells. (PubMed id 17932509)1, 2 Hoeck J.... Meister G. (2007)
    4. NMR structure of the three quasi RNA recognition motifs (qRRMs) of human hnRNP F and interaction studies with Bcl-x G-tract RNA: a novel mode of RNA recognition. (PubMed id 16885237)1, 2 Dominguez C. and Allain F.H. (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. Sumoylation of heterogeneous nuclear ribonucleoproteins, zinc finger proteins, and nuclear pore complex proteins: a proteomic analysis. (PubMed id 15161980)1, 2 Li T....Chock P.B. (2004)
    8. The DNA sequence and comparative analysis of human chromosome 10. (PubMed id 15164054)1, 2 Deloukas P.... Rogers J. (2004)
    9. 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)
    10. Purification and characterization of native spliceosomes suitable for three-dimensional structural analysis. (PubMed id 11991638)1, 2 Jurica M.S.... Moore M.J. (2002)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
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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: 3185 HGNC: 5039 AceView: HNRPF Ensembl:ENSG00000169813 euGenes: HUgn3185
    ECgene: HNRNPF H-InvDB: HNRNPF

    (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 HNRNPF 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 HNRNPF gene:
    Search GeneIP for patents involving HNRNPF

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



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