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

HNRNPAB Gene

protein-coding   GIFtS: 53
GCID: GC05P177631

heterogeneous nuclear ribonucleoprotein A/B


(Previous symbol: HNRPAB)
 Explore 12 diseases affiliated with
HNRNPAB via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for HNRNPAB    

Aliases
for HNRNPAB gene

(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 A/B1 2     HnRNP A/B2 3
ABBP11 2 3     FLJ403381
HNRPAB1 2 3     Apobec-1 Binding Protein 12
ABBP-12 3     Apolipoprotein B MRNA Editing Enzyme, Catalytic Polypeptide 1-Binding Protein 12
APOBEC1-Binding Protein 12 3     HnRNP Type A/B Protein2

External Ids:    HGNC: 50341   Entrez Gene: 31822   Ensembl: ENSG000001974517   OMIM: 6026885   UniProtKB: Q997293   

Export aliases for HNRNPAB gene to outside databases

Previous GC identifers: GC05P177565 GC05P172357


Summaries
for HNRNPAB gene

(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 HNRNPAB:
This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The
hnRNPs are produced by RNA polymerase II and are components of the heterogeneous nuclear RNA (hnRNA) complexes. They
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,
which binds to one of the components of the multiprotein editosome complex, has two repeats of quasi-RRM (RNA
recognition motif) domains that bind to RNAs. Two alternatively spliced transcript variants encoding different
isoforms have been described for this gene. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: ROAA_HUMAN, Q99729
Function: Binds single-stranded RNA. Has a high affinity for G-rich and U-rich regions of hnRNA. Also binds to APOB
mRNA transcripts around the RNA editing site

Gene Wiki entry for HNRNPAB (HNRPAB)


Genomic Views
for HNRNPAB 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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000005.9  NC_018916.1  NT_023133.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HNRNPAB gene promoter:
         Nkx2-5   CBF-C   CREB   CBF-A   CBF-B   deltaCREB   CP1C   CP1A   NF-Y   CBF(2)   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for HNRNPAB

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


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

Entrez Gene cytogenetic band: 5q35.3   Ensembl cytogenetic band:  5q35.3   HGNC cytogenetic band: 5q35.3

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

GeneLoc information about chromosome 5         GeneLoc Exon Structure

GeneLoc location for GC05P177631:  view genomic region     (about GC identifiers)

Start:
 177,631,508 bp from pter      End:
 177,638,184 bp from pter
Size:
 6,677 bases      Orientation:
 plus strand

Proteins
for HNRNPAB gene

(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: ROAA_HUMAN, Q99729 (See protein sequence)
Recommended Name: Heterogeneous nuclear ribonucleoprotein A/B  
Size: 332 amino acids; 36225 Da
Subunit: Identified in a mRNP granule complex, at least composed of ACTB, ACTN4, DHX9, ERG, HNRNPA1, HNRNPA2B1,
HNRNPAB, HNRNPD, HNRNPL, HNRNPR, HNRNPU, HSPA1, HSPA8, IGF2BP1, ILF2, ILF3, NCBP1, NCL, PABPC1, PABPC4, PABPN1, RPLP0,
RPS3, RPS3A, RPS4X, RPS8, RPS9, SYNCRIP, TROVE2, YBX1 and untranslated mRNAs. Interacts with APOBEC1
Subcellular location: Nucleus. Cytoplasm. Note=Localized in cytoplasmic mRNP granules containing untranslated mRNAs
Sequence caution: Sequence=AAC50956.1; Type=Frameshift; Positions=296, 307, 330;
1 PDB 3D structure from and Proteopedia for HNRNPAB:
3S7R (3D)    
Secondary accessions: B3KNN5 D3DWP7 Q04150 Q8N7U3 Q9BQ99
Alternative splicing: 4 isoforms:  Q99729-1   Q99729-2   Q99729-3   Q99729-4   (Ref.1 (AAA36575) sequence differs from that shown due to several frameshifts. Contains a N6-acetyllysine at position 272. Contains a phosphoserine at position 256)

Explore the universe of human proteins at neXtProt for HNRNPAB: NX_Q99729

Post-translational modifications:

  • Dimethylation at Arg-322 is probably asymmetric1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q99729

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

    REFSEQ proteins (2 alternative transcripts): 
    NP_004490.2  NP_112556.2  

    ENSEMBL proteins: 
     ENSP00000351108   ENSP00000422501   ENSP00000348093   ENSP00000427110   ENSP00000423495  
     ENSP00000427465   ENSP00000425031  

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    Uscn Proteins for HNRNPAB

    Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus ISS--
    GO:0005730NOT nucleolus IDA--
    GO:0005737cytoplasm ISS--
    GO:0030529ribonucleoprotein complex IDA17289661


    HNRNPAB for ontologies           About GeneDecksing



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    Protein Domains /
    Families
    for HNRNPAB gene

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

    3 InterPro domains/families:
     IPR012956 CARG-binding_factor_N
     IPR012677 Nucleotide-bd_a/b_plait
     IPR000504 RRM_dom

    Graphical View of Domain Structure for InterPro Entry Q99729

    ProtoNet protein and cluster: Q99729

    2 Blocks protein families:
    IPB000504 RNA-binding region RNP-1 (RNA recognition motif)
    IPB012956 CBF


    UniProtKB/Swiss-Prot: ROAA_HUMAN, Q99729
    Similarity: Contains 2 RRM (RNA recognition motif) domains


    Function
    for HNRNPAB gene

    (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: ROAA_HUMAN, Q99729
    Function: Binds single-stranded RNA. Has a high affinity for G-rich and U-rich regions of hnRNA. Also binds to APOB
    mRNA transcripts around the RNA editing site

    miRNA
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    hsa-miR-548m hsa-miR-3163 hsa-miR-1197 hsa-miR-376a* hsa-miR-548k hsa-miR-548n
    SwitchGear 3'UTR luciferase reporter plasmid: HNRNPAB 3' UTR sequence
    Inhib. RNA
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    Gene Editing
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    Clone
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    In Situ Assay
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    Gene Ontology (GO): 5/6 molecular function terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000166nucleotide binding IEA--
    GO:0003676nucleic acid binding ----
    GO:0003700contributes to sequence-specific DNA binding transcription factor activity ISS--
    GO:0003723RNA binding TAS1717314
    GO:0003729mRNA binding TAS8999813


    HNRNPAB for ontologies           About GeneDecksing


    3 GenomeRNAi human phenotypes for HNRNPAB:
     Decreased Hepatitis C virus re  Decreased viability of wild-ty  Synthetic lethal with c-Myc af 


    Pathways & Interactions
    for HNRNPAB gene

    (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 processing0.48


    1 BioSystems Pathway for HNRNPAB 
        mRNA processing


    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for HNRNPAB

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

    5/639 Interacting proteins for HNRNPAB (Q997292, 3 ENSP000003511084) via UniProtKB, MINT, STRING, and/or I2D (see all 639)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    ACTBP607092, 3, ENSP000003499604MINT-7945693 I2D: score=2 STRING: ENSP00000349960
    SF3A2Q154282, 3, ENSP000002214944MINT-5205818 I2D: score=1 STRING: ENSP00000221494
    NSFP464592, 3MINT-7945693 I2D: score=1 
    SQSTM1Q135012, 3MINT-7945693 I2D: score=1 
    SYNCRIPO605062, 3MINT-7945693 I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001837epithelial to mesenchymal transition ISS--
    GO:0045893positive regulation of transcription, DNA-dependent ISS--


    HNRNPAB for ontologies           About GeneDecksing



    Drugs & Compounds
    for HNRNPAB gene

    (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 HNRNPAB
    Search CenterWatch for drugs/clinical trials and news about HNRNPAB / ROAA 

    Transcripts
    for HNRNPAB gene

    (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, 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 HNRNPAB gene (2 alternative transcripts): 
    NM_004499.3  NM_031266.2  

    Unigene Cluster for HNRNPAB:

    Heterogeneous nuclear ribonucleoprotein A/B
    Hs.591731  [show with all ESTs]
    Unigene Representative Sequence: NM_031266
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000358344(uc003miu.3 uc003miv.3) ENST00000506339 ENST00000355836
    ENST00000514633 ENST00000515193 ENST00000506259(uc003mix.3) ENST00000504898
    ENST00000504796

    miRNA
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    6 QIAGEN miScript miRNA Assays for microRNAs that regulate HNRNPAB:
    hsa-miR-548m hsa-miR-3163 hsa-miR-1197 hsa-miR-376a* hsa-miR-548k hsa-miR-548n
    SwitchGear 3'UTR luciferase reporter plasmid: HNRNPAB 3' UTR sequence
    Inhib. RNA
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    Clone
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    Primer
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat HNRNPAB
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    Additional cDNA sequence: 

    AK054600.1 AK097657.1 AK223425.1 BC001616.1 BC002625.2 BC004561.2 BC009359.2 BC015556.2 
    BC036708.2 M65028.1 U76713.1 Z36844.1 

    23 DOTS entries:

    DT.446996  DT.100839425  DT.100839434  DT.91762877  DT.100839418  DT.100839441  DT.120839439  DT.100044721 
    DT.120839602  DT.40287340  DT.120839512  DT.95184714  DT.121137298  DT.100839440  DT.120839523  DT.120839610 
    DT.95235931  DT.100044720  DT.120839530  DT.120839552  DT.446995  DT.100682262  DT.95184703 

    24/647 AceView cDNA sequences (see all 647):

    BQ066259 BM840302 BG683586 BQ923791 CR602810 BQ940610 BQ068738 BM853528 
    BC004561 AA827225 AV708780 BC009359 BQ065884 BQ060866 CR610440 BQ430329 
    BU145952 BQ029236 BC001616 CR609806 BG291815 AA552446 AW243988 CR623272 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for HNRNPAB    About this scheme

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


    ECgene alternative splicing isoforms for HNRNPAB

    Expression
    for HNRNPAB gene

    (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

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

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)
    About this image
    See HNRNPAB Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for HNRNPAB

    SOURCE GeneReport for Unigene cluster: Hs.591731

    UniProtKB/Swiss-Prot: ROAA_HUMAN, Q99729
    Tissue specificity: Ubiquitous

        SABiosciences Custom PCR Arrays for HNRNPAB
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    In Situ
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    Orthologs
    for HNRNPAB gene

    (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 animals.

    Orthologs for HNRNPAB gene from 6/18 species (see all 18)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    mouse
    (Mus musculus)    		 Mammalia Hnrnpab1 , 5 heterogeneous nuclear ribonucleoprotein A/B1, 5 91.03(n)1
    94.19(a)1    		   11 (31.11 cM)5
    153841  NM_001048061.11  NP_001041526.11 
     516001005 
    chicken
    (Gallus gallus)    		 Aves HNRNPAB1 heterogeneous nuclear ribonucleoprotein A/B 77.22(n)
    85.41(a)    		   396268  NM_205328.4  NP_990659.1 
    lizard
    (Anolis carolinensis)    		 Reptilia HNRNPAB6
    		 --
    		 76(a)
    		 1 ↔ 1
    		 2(142037702-142045288)
    African clawed frog
    (Xenopus laevis)    		 Amphibia hnrpab-prov2 heterogeneous nuclear ribonucleoprotein A/B 82.16(n)    BC043814.1 
    zebrafish
    (Danio rerio)    		 Actinopterygii Dr.188362 Danio rerio mRNA similar to heterogeneous nuclear ribonucleoprotein more 78.91(n)    BC048898.1 
    fruit fly
    (Drosophila melanogaster)    		 Insecta sqd1 squid 54.24(n)
    46.13(a)    		   41666  NM_169528.2  NP_731825.1 


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

    Paralogs
    for HNRNPAB gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HNRNPAB gene
    HNRNPA32  DAZAP12  HNRNPA2B12  HNRNPA1L22  MSI12  HNRNPD2  HNRNPA12  HNRNPA02  
    MSI22  HNRPDL2  
    17 SIMAP similar genes for HNRNPAB using alignment to 4 protein entries:     ROAA_HUMAN (see all proteins):
    HNRPDL    HNRNPD    HNRNPA2B1    HNRPA1    HNRNPA1    HNRNPA1L2
    HNRPA3    MSI2    HNRNPA3    D10S102    MSI1    SLIRP
    HNRNPA0    DAZAP1    RBMY1A1    CIRBP    RBM38

    HNRNPAB for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for HNRNPAB
    PGOHUM00000239668


    Genomic Variants
    for HNRNPAB gene

    (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

    10/204 NCBI SNPs in HNRNPAB are shown (see all 204)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr 5 posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs49767151,2
    		C,--177629543(+) GGCAGA/GAGAAT 2 -- us2k10--------
    rs21150531,2
    		C,A,H,--177629559(+) GAACCC/TGGGAG 2 -- us2k17Minor allele frequency- T:0.00NA WA CSA 13
    rs348313571,2
    		C,--177629640(+) CAAAG-/AAAAAA 2 -- us2k12Minor allele frequency- A:0.00NA CSA 4
    rs1408212051,2
    		--177629661(+) GATCTA/GGCTGG 2 -- us2k10--------
    rs1173564841,2
    		--177629676(+) CATAGG/AGAGAC 2 -- us2k11Minor allele frequency- A:0.01EA 120
    rs1447483881,2
    		C,--177629691(+) TTTAC-/AAAAAA 2 -- us2k10--------
    rs29616731,2
    		C,F,--177629801(+) gtgatC/Ggtgcc 2 -- us2k1 tfbs36Minor allele frequency- G:0.24WA NA CSA 246
    rs1819925171,2
    		--177629808(+) TGCCAC/GTGGAC 2 -- us2k10--------
    rs1399482391,2
    		C,--177629849(+) GTCAA-/AAAAT 
                AAAAT     		2 -- us2k10--------
    rs1501311531,2
    		--177629915(+) AGAAAA/GTGGAA 2 -- us2k10--------

    HapMap Linkage Disequilibrium report for HNRNPAB (177631508 - 177638184 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for HNRNPAB
         1 CNV: 59251

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    Disorders / Diseases
    for HNRNPAB gene

    (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
    HNRNPAB for disorders           About GeneDecksing

    OMIM gene information: 602688    OMIM disorders: --

    12 diseases for HNRNPAB:    About MalaCards
    hay-wells syndrome    hallervorden-spatz syndrome    wells syndrome    cystic fibrosis
    fibrosis    hepatocellular carcinoma    pancreatic cancer    pancreatitis
    immunodeficiency    carcinoma    malaria    neuronitis


    Export disorders for HNRNPAB gene to outside databases

    Publications
    for HNRNPAB gene

    (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 HNRNPAB gene, integrated from 9 sources (see all 58):
    (articles sorted by number of sources associating them with HNRNPAB)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Cloning and sequence analysis of a human type A/B hnRNP protein. (PubMed id 1717314)1, 2, 3 Khan F.... Szer W. (1991)
    2. Cloning of an Apobec-1-binding protein that also interacts with apolipoprotein B mRNA and evidence for its involvement in RNA editing. (PubMed id 8999813)1, 2, 9 Lau P.P.... Chan L. (1997)
    3. Molecular composition of IMP1 ribonucleoprotein granules. (PubMed id 17289661)1, 2 Joeson L.... Nielsen F.C. (2007)
    4. A probability-based approach for high-throughput protein phosphorylation analysis and site localization. (PubMed id 16964243)1, 2 Beausoleil S.A.... Gygi S.P. (2006)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    6. Identifying and quantifying in vivo methylation sites by heavy methyl SILAC. (PubMed id 15782174)1, 2 Ong S.E.... Mann M. (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. P63 alpha mutations lead to aberrant splicing of keratinocyte growth factor receptor in the Hay-Wells syndrome. (PubMed id 12692135)1, 9 Fomenkov A....Ratovitski E. (2003)
    9. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    10. Host cell interactome of HIV-1 Rev includes RNA helica ses involved in multiple facets of virus production. (PubMed id 22174317)1 Naji S....Gerace L. (2012)

    External Searches for HNRNPAB gene

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
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    Genome Databases showing HNRNPAB gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 3182 HGNC: 5034 AceView: HNRPAB Ensembl:ENSG00000197451 euGenes: HUgn3182
    ECgene: HNRNPAB H-InvDB: HNRNPAB

    Other Databases showing HNRNPAB gene

    (According to HUGE)
    About This Section
    		   --

    Specialized Databases showing HNRNPAB gene

    (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 HNRNPAB Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for HNRNPAB gene

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

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



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