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

ARHGAP18 Gene

protein-coding   GIFtS: 52
GCID: GC06M129897

Rho GTPase activating protein 18

 Explore 4 diseases affiliated with
ARHGAP18 via our new
 Human Malady Compendium 
Biological research products
for ARHGAP18
    

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

Aliases
Rho GTPase Activating Protein 181 2
MacGAP1 2 3
BA307O14.21
Rho-Type GTPase-Activating Protein 182 3
SENEX2
Rho GTPase-Activating Protein 182

External Ids:    HGNC: 210351   Entrez Gene: 936632   Ensembl: ENSG000001463767   OMIM: 6133515   UniProtKB: Q8N3923   

Export aliases for ARHGAP18 gene to outside databases

Previous GC identifers: GC06M129832 GC06M129878 GC06M129939 GC06M127478


(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 ARHGAP18:
ARHGAP18 belongs to a family of Rho (see MIM 165390) GTPase-activating proteins that modulate cell signaling (Potkin et
al., 2009 (PubMed 19065146)).(supplied by OMIM, Apr 2010)

UniProtKB/Swiss-Prot: RHG18_HUMAN, Q8N392
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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000006.11  NC_018917.1  NT_025741.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ARHGAP18 gene promoter:
         TBP   RORalpha1   SRY   S8   SREBP-1a   FOXJ2 (long isoform)   Chx10   FOXJ2   SREBP-1b   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidARHGAP18 promoter sequence
   Search SABiosciences Chromatin IP Primers for ARHGAP18

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ARHGAP18


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

Entrez Gene cytogenetic band: 6q22.33   Ensembl cytogenetic band:  6q22.33   HGNC cytogenetic band: 6q23.1

ARHGAP18 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ARHGAP18 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M129897:  view genomic region     (about GC identifiers)

Start:
129,897,277 bp from pter      End:
130,031,370 bp from pter
Size:
134,094 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: RHG18_HUMAN, Q8N392 (See protein sequence)
Recommended Name: Rho GTPase-activating protein 18  
Size: 663 amino acids; 74977 Da
Subunit: Interacts with MPHOSPH6
Sequence caution: Sequence=AAH17223.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Potential poly-A
sequence; Sequence=AAH39611.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Potential poly-A sequence;
Sequence=AAH62417.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Potential poly-A sequence;
Sequence=BAB61887.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
Secondary accessions: E1P575 Q58EZ3 Q6P679 Q6PJD7 Q96S64
Alternative splicing: 2 isoforms:  Q8N392-1   Q8N392-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ARHGAP18: NX_Q8N392

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8N392

  • ARHGAP18 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_277050.2  
    ENSEMBL proteins: 
     ENSP00000357131   ENSP00000275189  
    Reactome Protein details: Q8N392
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    Uscn Proteins for ARHGAP18

    Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005829cytosol TAS--


    ARHGAP18 for ontologies           About GeneDecksing



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

    ARHGAP18 for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR008936 Rho_GTPase_activation_prot
     IPR000198 RhoGAP_dom

    Graphical View of Domain Structure for InterPro Entry Q8N392

    ProtoNet protein and cluster: Q8N392

    1 Blocks protein family: IPB000198 RhoGAP domain

    UniProtKB/Swiss-Prot: RHG18_HUMAN, Q8N392
    Similarity: Contains 1 Rho-GAP domain


    (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: RHG18_HUMAN, Q8N392
    Function: GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state (By similarity)

    miRNA
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    hsa-miR-3163 hsa-miR-3128 hsa-miR-4251 hsa-miR-499-3p hsa-miR-183 hsa-miR-944 hsa-miR-335 hsa-miR-548l
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005096GTPase activator activity IEA--


    ARHGAP18 for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for ARHGAP18:
     Decreased viability with pacli  Synthetic lethal with Ras 

    Animal Models:
         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Arhgap18):
     mortality/aging 

    ARHGAP18 for phenotypes           About GeneDecksing


    (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
    1Cell death signalling via NRAGE, NRIF and NADE
    Signaling by Rho GTPases0.25
    Rho GTPase cycle0.25
    2Signaling by GPCR
    Signal Transduction0.56

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    3        Reactome Pathways for ARHGAP18
        Signaling by Rho GTPases
    Signal Transduction
    Rho GTPase cycle



    ARHGAP18 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ARHGAP18

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

    5/36 Interacting proteins for ARHGAP18 (Q8N3923 ENSP000002751894) via UniProtKB, MINT, STRING, and/or I2D (see all 36)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    MPP6Q9NZW53, ENSP000002226444I2D: score=2 STRING: ENSP00000222644
    MPHOSPH6Q995473, ENSP000002581694I2D: score=3 STRING: ENSP00000258169
    ARHGAP4ENSP000002037864STRING: ENSP00000203786
    ARHGDIAENSP000002693214STRING: ENSP00000269321
    ARHGEF2ENSP000003153254STRING: ENSP00000315325
    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:0007264small GTPase mediated signal transduction TAS--
    GO:0051056regulation of small GTPase mediated signal transduction TAS--


    ARHGAP18 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 ARHGAP18
    Search CenterWatch for drugs/clinical trials and news about ARHGAP18 / RHG18 

    (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 ARHGAP18 gene: 
    NM_033515.2  

    Unigene Cluster for ARHGAP18:

    Rho GTPase activating protein 18
    Hs.486458  [show with all ESTs]
    Unigene Representative Sequence: NM_033515
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000368149 ENST00000483367 ENST00000463225 ENST00000275189(uc003qbr.3 uc011ebw.2 uc021zfe.1)


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    hsa-miR-3163 hsa-miR-3128 hsa-miR-4251 hsa-miR-499-3p hsa-miR-183 hsa-miR-944 hsa-miR-335 hsa-miR-548l
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    Additional cDNA sequence: 

    AB053293.1 AK002195.1 AK098594.1 AK307796.1 AL834511.1 AY643712.1 BC017223.2 BC039611.1 
    BC052295.1 BC062417.1 BC073143.1 BC101708.1 BC107416.1 BC111940.1 BC143531.1 

    5 DOTS entries:

    DT.107983  DT.121328540  DT.100035030  DT.121328539  DT.121328566 

    24/155 AceView cDNA sequences (see all 155):

    BC052295 BG031862 AA490588 BM980534 AA421756 AA357393 BQ430412 BQ029517 
    CA449202 BF431069 BM557178 BU752916 BM721946 BU664426 AI827394 BQ129374 
    AW612901 AA736655 AI783545 CB133859 AW157785 AA669517 AB053293 AL834511 

    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™, 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

    ARHGAP18 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: ATGCCGCCAG

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

    About this image
    See ARHGAP18 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ARHGAP18

    SOURCE GeneReport for Unigene cluster: Hs.486458
        SABiosciences Custom PCR Arrays for ARHGAP18
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ARHGAP18

    (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 ARHGAP18 gene from 5/18 species (see all 18)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves ARHGAP181 Rho GTPase activating protein 18 74.68(n)
    75.04(a)
      421706  XM_419743.3  XP_419743.3 
    lizard
    (Anolis carolinensis)
    Reptilia ARHGAP186
    --
    69(a)
    1 ↔ 1
    GL343315.1(683744-718408)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.181242 Xenopus laevis transcribed sequence with moderate similarity more 77.1(n)    BG885983.1 
    zebrafish
    (Danio rerio)
    Actinopterygii LOC1000042521 rho GTPase-activating protein 18-like 58.35(n)
    57.03(a)
      100004252  XM_001343565.4  XP_001343601.4 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG170826
    --
    16(a)
    1 → many
    2R(631836-645548)


    ENSEMBL Gene Tree for ARHGAP18 (if available)
    TreeFam Gene Tree for ARHGAP18 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ARHGAP18 gene
    ARHGAP362  ARHGAP62  STARD132  ARHGAP402  ARHGAP11A2  DLC12  ARHGAP282  ARHGAP11B2  
    STARD82  
    4 SIMAP similar genes for ARHGAP18 using alignment to 1 protein entry:     RHG18_HUMAN:
    ARHGAP12    ARHGAP28    ARHGAP40    ARHGAP9

    ARHGAP18 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/2441 NCBI SNPs in ARHGAP18 are shown (see all 2441    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1140736921,2
    F,--129897810(+) CAAACG/ATTGCG 1 -- int11Minor allele frequency- A:0.06WA 118
    rs1932305401,2
    --129897844(+) GACAAC/GCTTTT 1 -- int10--------
    rs1839194031,2
    --129897849(+) CCTTTA/TACTTA 1 -- int10--------
    rs1136802681,2
    C,--129897875(+) CTATCT/-TTTTT 1 -- int11Minor allele frequency- -:0.50CSA 2
    rs1881500051,2
    --129897928(+) TTTTCC/TTTTAT 1 -- int10--------
    rs1413448971,2
    --129897980(+) TAATTA/GGGAAA 1 -- int10--------
    rs1813498351,2
    --129898048(+) AAAATG/TTGTAA 1 -- int10--------
    rs1135727991,2
    --129898072(+) AAAGAC/TGAAAA 1 -- int12Minor allele frequency- T:0.04CSA WA 120
    rs1507855331,2
    --129898133(+) GAAAAC/TAGAGG 1 -- int10--------
    rs1380396651,2
    --129898168(+) ATTTCG/TCAATA 1 -- int10--------

    HapMap Linkage Disequilibrium report for ARHGAP18 (129897277 - 130031370 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 5 variations for ARHGAP18
         1 CNV: 4507
         4 Indels: 28093 28091 99706 28092

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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

    ARHGAP18 for disorders           About GeneDecksing

    OMIM gene information: 613351    OMIM disorders: --

    4 diseases for ARHGAP18:    About MalaCards
    intellectual disability    intrahepatic cholangiocarcinoma    cholangiocarcinoma    schizophrenia

    1 disease from the University of Copenhagen DISEASES database for ARHGAP18:
    Intellectual disability
    Human Genome Epidemiology (HuGE) Navigator: ARHGAP18 (3 documents)

    Export disorders for ARHGAP18 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 ARHGAP18 gene, integrated from 9 sources (see all 13):
    (articles sorted by number of sources associating them with ARHGAP18)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. A protein interaction framework for human mRNA degradation. (PubMed id 15231747)1, 2 Lehner B. and Sanderson C.M. (2004)
    2. 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)
    3. The DNA sequence and analysis of human chromosome 6. (PubMed id 14574404)1, 2 Mungall A.J.... Beck S. (2003)
    4. Genetically distinct subsets within ANCA-associated va sculitis. (PubMed id 22808956)1 Lyons P.A....Smith K.G. (2012)
    5. ARHGAP18, a GTPase-activating protein for RhoA, contr ols cell shape, spreading, and motility. (PubMed id 21865595)1 Maeda M....Senga T. (2011)
    6. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)
    7. Stress-induced premature senescence mediated by a nov el gene, SENEX, results in an anti-inflammatory phenotype in endothelial cells. (PubMed id 20664062)1 Coleman P.R....Gamble J.R. (2010)
    8. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia. (PubMed id 19065146)1 Potkin S.G....Macciardi F. (2009)
    9. Screening for replication of genome-wide SNP associations in sporadic ALS. (PubMed id 18987618)1 Cronin S....Hardiman O. (2008)
    10. The full-ORF clone resource of the German cDNA consortium. (PubMed id 17974005)2 Bechtel S.... Schupp I. (2007)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 93663 HGNC: 21035 AceView: ARHGAP18 Ensembl:ENSG00000146376 euGenes: HUgn93663
    ECgene: ARHGAP18 H-InvDB: ARHGAP18

    (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 ARHGAP18 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 ARHGAP18 gene:
    Search GeneIP for patents involving ARHGAP18

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



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