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ARHGAP28 Gene

protein-coding   GIFtS: 51
GCID: GC18P006730

Rho GTPase Activating Protein 28

  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Rho GTPase Activating Protein 281 2
Rho-Type GTPase-Activating Protein 282 3
KIAA13143 5
Rho GTPase-Activating Protein 282

External Ids:    HGNC: 255091   Entrez Gene: 798222   Ensembl: ENSG000000887567   OMIM: 6105925   UniProtKB: Q9P2N23   

Export aliases for ARHGAP28 gene to outside databases

Previous GC identifers: GC18P006781 GC18U900243


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for ARHGAP28 Gene:
ARHGAP28 (Rho GTPase activating protein 28) is a protein-coding gene. Diseases associated with ARHGAP28 include benign meningioma, and meningioma. GO annotations related to this gene include GTPase activator activity. An important paralog of this gene is ARHGAP36.

UniProtKB/Swiss-Prot: RHG28_HUMAN, Q9P2N2
Function: GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state (By
similarity)




(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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence:
NC_000018.10  NT_010859.15  NC_018929.2  
Regulatory elements:
   Regulatory transcription factor binding sites in the ARHGAP28 gene promoter:
         TBP   STAT5B   AML1a   STAT5A   Nkx2-5   NF-AT   FOXC1   POU2F1   POU2F1a   NF-AT1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidARHGAP28 promoter sequence
   Search Chromatin IP Primers for ARHGAP28

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat ARHGAP28


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

Entrez Gene cytogenetic band: 18p11.31   Ensembl cytogenetic band:  18p11.31   HGNC cytogenetic band: 18p11.23

ARHGAP28 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ARHGAP28 gene location

GeneLoc information about chromosome 18         GeneLoc Exon Structure

GeneLoc location for GC18P006730:  view genomic region     (about GC identifiers)

Start:
6,729,717 bp from pter      End:
6,915,715 bp from pter
Size:
185,999 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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., Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: RHG28_HUMAN, Q9P2N2 (See protein sequence)
Recommended Name: Rho GTPase-activating protein 28  
Size: 729 amino acids; 82060 Da
Sequence caution: Sequence=BAA91533.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
Sequence=BAA92552.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;
Secondary accessions: A8MQB7 A8MU88 Q6P160 Q8N4T3 Q9NW53
Alternative splicing: 4 isoforms:  Q9P2N2-1   Q9P2N2-2   Q9P2N2-3   Q9P2N2-5   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ARHGAP28: NX_Q9P2N2

Explore proteomics data for ARHGAP28 at MOPED

Post-translational modifications: 

  • Modification sites at neXtProt
  • Modification sites at PhosphoSitePlus

  • See ARHGAP28 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

    REFSEQ proteins: NP_001010000.1  
    ENSEMBL proteins: 
     ENSP00000372964   ENSP00000464141   ENSP00000462831   ENSP00000433390   ENSP00000262227  
     ENSP00000462912   ENSP00000392660   ENSP00000437262   ENSP00000464310   ENSP00000463672  
     ENSP00000435990   ENSP00000463143   ENSP00000382963   ENSP00000313506   ENSP00000406907  
    Reactome Protein details: Q9P2N2

    ARHGAP28 Human Recombinant Protein Products:

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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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    HGNC Gene Families:
    ARHGAP: Rho GTPase activating proteins

    2 InterPro protein domains:
     IPR008936 Rho_GTPase_activation_prot
     IPR000198 RhoGAP_dom

    Graphical View of Domain Structure for InterPro Entry Q9P2N2

    ProtoNet protein and cluster: Q9P2N2

    1 Blocks protein domain: IPB000198 RhoGAP domain

    UniProtKB/Swiss-Prot: RHG28_HUMAN, Q9P2N2
    Similarity: Contains 1 Rho-GAP domain


    ARHGAP28 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,
    transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Molecular Function:

         UniProtKB/Swiss-Prot Summary: RHG28_HUMAN, Q9P2N2
    Function: GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state (By
    similarity)

         Gene Ontology (GO): 1 molecular function term:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005096GTPase activator activity IEA--
         
    ARHGAP28 for ontologies           About GeneDecksing


    Phenotypes:
         2 GenomeRNAi human phenotypes for ARHGAP28:
     Downregulation of NF-kappaB pa  Downregulation of NF-kappaB pa 

    Animal Models:
       inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for ARHGAP28
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    hsa-mir-98-5p (MIRT027425), hsa-mir-196a-5p (MIRT026097), hsa-mir-124-3p (MIRT022171)

    Block miRNA regulation of human, mouse, rat ARHGAP28 using miScript Target Protectors
    Selected qRT-PCR Assays for microRNAs that regulate ARHGAP28 (see all 25):
    hsa-miR-579 hsa-miR-875-3p hsa-let-7d hsa-miR-202 hsa-miR-767-5p hsa-let-7c hsa-miR-507 hsa-let-7g
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    (According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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    Subcellular locations from COMPARTMENTS: 

    CompartmentConfidence
    cytosol4
    nucleus4

    Gene Ontology (GO): 5 cellular component terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular ----
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0005829cytosol TAS--
    GO:0030054cell junction IDA--

    ARHGAP28 for ontologies           About GeneDecksing


    (SuperPaths according to PathCards, Pathways according to 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 QIAGEN, 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 Apr 2014 via Entrez Gene).
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    SuperPaths for ARHGAP28 About    
    See pathways by source

    SuperPathContained pathways About
    1Rho GTPase cycle
    Rho GTPase cycle1.00
    Signaling by Rho GTPases1.00
    2Signaling by GPCR
    Signal Transduction0.58

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    1 Reactome Pathway for ARHGAP28
        Rho GTPase cycle



    ARHGAP28 for pathways           About GeneDecksing

        Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for ARHGAP28
    Interactions:

        Search GeneGlobe Interaction Network for ARHGAP28

    Gene Ontology (GO): 3 biological process terms:    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007165signal transduction ----
    GO:0007264small GTPase mediated signal transduction TAS--
    GO:0051056regulation of small GTPase mediated signal transduction TAS--

    ARHGAP28 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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    Browse Small Molecules at EMD Millipore
       Browse drugs & compounds from Enzo Life Sciences
      Browse compounds at ApexBio 

    Browse Tocris compounds for ARHGAP28 (RHG28)



    (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,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
    Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, and/or QIAGEN )
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    REFSEQ mRNAs for ARHGAP28 gene (2 alternative transcripts): 
    NM_030672.2  NM_001010000.2  

    Unigene Cluster for ARHGAP28:

    Rho GTPase activating protein 28
    Hs.183114  [show with all ESTs]
    Unigene Representative Sequence: NM_001010000
    17 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000383472 ENST00000583410 ENST00000584387 ENST00000532723 ENST00000262227(uc002knc.3)
    ENST00000581099 ENST00000419673(uc002kne.3 uc010wzi.2) ENST00000531294
    ENST00000584287 ENST00000577524 ENST00000532996(uc002knf.3) ENST00000579689
    ENST00000579245 ENST00000579796 ENST00000400091 ENST00000314319 ENST00000418986

    miRNA
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    Selected qRT-PCR Assays for microRNAs that regulate ARHGAP28 (see all 25):
    hsa-miR-579 hsa-miR-875-3p hsa-let-7d hsa-miR-202 hsa-miR-767-5p hsa-let-7c hsa-miR-507 hsa-let-7g
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    Additional mRNA sequence: 

    AB037735.1 AK001174.1 AK024298.1 AK289791.1 AK302026.1 AK308259.1 BC033668.1 BC065274.1 
    BX648684.1 

    10 DOTS entries:

    DT.410248  DT.100728701  DT.100022141  DT.92419891  DT.121087962  DT.101969868  DT.121087973  DT.65284146 
    DT.75115625  DT.95268365 

    GeneLoc Exon Structure


    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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    ARHGAP28 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: ACACTAGAAA
    ARHGAP28 Expression
    About this image


    ARHGAP28 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database
     selected tissues (see all 7) fully expand
     
     Testis (Reproductive System)
             Testis Somatic Cells Primitive Gonad
     
     Paraxial Mesoderm (Gastrulation Derivatives)
             PureStem SK11, NCr-fac & Meso-prx Progenitor
     
     Neural Crest (Gastrulation Derivatives)
             PureStem SK11, NCr-fac & Meso-prx Progenitor
     
     Heart (Cardiovascular System)
             Cardiac Fibroblasts Myocardium
     
     Fibroblasts
             Cardiac Fibroblasts Myocardium
    ARHGAP28 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

    ARHGAP28 Protein Expression

    SOURCE GeneReport for Unigene cluster: Hs.183114

    UniProtKB/Swiss-Prot: RHG28_HUMAN, Q9P2N2
    Tissue specificity: Expressed in testis. Expressed at moderate level in kidney and ovary, and weakly expressed in
    spleen and skeletal muscle

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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)
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    This gene was present in the common ancestor of animals.

    Orthologs for ARHGAP28 gene from Selected species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Arhgap281 , 5 Rho GTPase activating protein 281, 5 83.42(n)1
    85.13(a)1
      17 (38.90 cM)5
    2689701  NM_172964.41  NP_766552.31 
     678427135 
    chicken
    (Gallus gallus)
    Aves ARHGAP281 Rho GTPase activating protein 28 67.15(n)
    59.75(a)
      421053  XM_419140.4  XP_419140.3 
    lizard
    (Anolis carolinensis)
    Reptilia ARHGAP286
    Rho GTPase activating protein 28
    45(a)
    1 ↔ 1
    GL343431.1(12784-41019)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia arhgap281 Rho GTPase activating protein 28 64.78(n)
    59(a)
      100488165  XM_002938054.2  XP_002938100.2 
    zebrafish
    (Danio rerio)
    Actinopterygii arhgap281 Rho GTPase activating protein 28 54.88(n)
    48.47(a)
      492794  NM_001007435.1  NP_001007436.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG170826
    --
    17(a)
    1 → many
    2R(631836-645548)


    ENSEMBL Gene Tree for ARHGAP28 (if available)
    TreeFam Gene Tree for ARHGAP28 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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    Paralogs for ARHGAP28 gene
    ARHGAP362  STARD132  ARHGAP62  ARHGAP402  ARHGAP182  DLC12  ARHGAP11A2  ARHGAP11B2  
    STARD82  
    5 SIMAP similar genes for ARHGAP28 using alignment to 10 protein entries:     RHG28_HUMAN (see all proteins):
    ARHGAP18    ARHGAP40    FAM13B    ARHGAP12    FAM13A

    ARHGAP28 for paralogs           About GeneDecksing



    (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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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    Selected SNPs for ARHGAP28 (see all 1809)    About this table    
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 18 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs733827981,2
    C,F--6832471(+) TTGATT/ATAACA 1 -- us2k11Minor allele frequency- A:0.50WA 2
    rs1836476071,2
    --6832607(+) ATTGTC/TACTCC 1 -- us2k10--------
    rs1449971701,2
    --6832611(+) TTACTC/GCTTGT 1 -- us2k10--------
    rs1165313301,2
    F--6832765(+) TATTTC/TATCCA 1 -- us2k11Minor allele frequency- T:0.04WA 118
    rs9715291,2
    C,F,A,H--6832779(-) aggtaG/Aagagt 1 -- us2k1113Minor allele frequency- A:0.31NS EA NA PA EU CA WA CSA 6922
    rs9715281,2
    C,F,H--6832832(-) GAAATG/ATAAGC 1 -- us2k191Minor allele frequency- A:0.01NS EA NA PA EU CA WA CSA 4593
    rs2020036001,2
    --6833067(+) TTGCT-/TTAAG 
            
    TTGTC
    1 -- us2k10--------
    rs775756091,2
    C--6833140(+) GTACAA/GTTTTA 1 -- us2k10--------
    rs1902465151,2
    --6833197(+) TCTATC/TACTCC 1 -- us2k10--------
    rs1486771401,2
    --6833263(+) CCATTC/TGCTGT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for ARHGAP28 (6729717 - 6915715 bp)

    Structural Variations
         Database of Genomic Variants (DGV) Selected variations for ARHGAP28 (see all 11):    About this table    
    Variant IDTypeSubtypePubMed ID
    esv2673830CNV Deletion23128226
    esv271900CNV Insertion20981092
    nsv132229CNV Insertion16902084
    nsv9604CNV Loss18304495
    nsv9605CNV Loss18304495
    nsv909337CNV Loss21882294
    esv27738CNV Gain19812545
    nsv909336CNV Gain21882294
    esv34611CNV Gain17911159
    nsv833583CNV Gain17160897

    Site Specific Mutation Identification with PCR Assays
    SeqTarget long-range PCR primers for resequencing ARHGAP28
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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.)
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    OMIM gene information: 610592    OMIM disorders: --

    4 diseases for ARHGAP28:    
    About MalaCards
    benign meningioma    meningioma    coronary artery disease    obesity

    1 disease from the University of Copenhagen DISEASES database for ARHGAP28:
    Benign meningioma

    ARHGAP28 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ARHGAP28

    Export disorders for ARHGAP28 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)
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    PubMed articles for ARHGAP28 gene, integrated from 10 sources (see all 11):
    (articles sorted by number of sources associating them with ARHGAP28)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro. (PubMed id 10718198)1, 2, 3 Nagase T.... Ohara O. (DNA Res. 2000)
    2. DNA sequence and analysis of human chromosome 18. (PubMed id 16177791)1, 2 Nusbaum C.... Lander E.S. (Nature 2005)
    3. 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. (Genome Res. 2004)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (Nat. Genet. 2004)
    5. Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (PubMed id 23251661)1 Comuzzie A.G....Butte N.F. (PLoS ONE 2012)
    6. System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation. (PubMed id 21406692)2 Rigbolt K.T....Blagoev B. (Sci. Signal. 2011)
    7. GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. (PubMed id 21658281)4 Aouizerat B.E....Tseng Z.H. (BMC Cardiovasc Disord 2011)
    8. Toward a confocal subcellular atlas of the human proteome. (PubMed id 18029348)1 Barbe L....Andersson-Svahn H. (amp 2008)
    9. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. (PubMed id 17903299)4 Kathiresan S....Cupples L.A. (BMC Med. Genet. 2007)
    10. The full-ORF clone resource of the German cDNA consortium. (PubMed id 17974005)2 Bechtel S.... Schupp I. (BMC Genomics 2007)

    (in PubMed, OMIM, and NCBI Bookshelf)
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     ANDOR
    Aliases
    Free Text  

      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)
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    Entrez Gene: 79822 HGNC: 25509 Ensembl:ENSG00000088756 euGenes: HUgn79822 ECgene: ARHGAP28
    H-InvDB: ARHGAP28

    (According to HUGE)
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    HUGE: KIAA1314

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
    About This Section

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    NameDescription
    PharmGKB entry for ARHGAP28 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
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    Patent Information for ARHGAP28 gene:
    Search GeneIP for patents involving ARHGAP28

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, and ESI BIO, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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