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

ARHGAP11B Gene

protein-coding   GIFtS: 38
GCID: GC15P030918

Rho GTPase activating protein 11B

(Previous names: family with sequence similarity 7, member B1 )
(Previous symbol: FAM7B1)
 Explore 1 disease affiliated with
ARHGAP11B via our new
 Human Malady Compendium 
Biological research products
for ARHGAP11B
    

(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 11B1 2     Rho-Type GTPase-Activating Protein 11B2 3
B'-T1 2     GAP (1-8)2
FAM7B11 2     Rho GTPase-Activating Protein 11B2
Family With Sequence Similarity 7, Member B11 2     

External Ids:    HGNC: 157821   Entrez Gene: 898392   Ensembl: ENSG000001879517   UniProtKB: Q3KRB83   

Export aliases for ARHGAP11B gene to outside databases

Previous GC identifers: GC00U917803 GC15P028707 GC15P008099


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

  --

(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_000015.9  NC_018926.1  NT_010194.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ARHGAP11B gene promoter:
         C/EBPbeta   AML1a   Nkx2-2   ATF-2   LCR-F1   PPAR-alpha   POU2F1   POU2F1a   FOXJ2 (long isoform)   FOXJ2   
         Other transcription factors

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Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ARHGAP11B


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

Entrez Gene cytogenetic band: 15q13.2   Ensembl cytogenetic band:  15q13.2   HGNC cytogenetic band: 15q13.2

ARHGAP11B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ARHGAP11B gene location

GeneLoc information about chromosome 15         GeneLoc Exon Structure

GeneLoc location for GC15P030918:  view genomic region     (about GC identifiers)

Start:
30,916,697 bp from pter      End:
31,060,329 bp from pter
Size:
143,633 bases      Orientation:
plus 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: RHGBB_HUMAN, Q3KRB8 (See protein sequence)
Recommended Name: Rho GTPase-activating protein 11B  
Size: 267 amino acids; 30251 Da

Explore the universe of human proteins at neXtProt for ARHGAP11B: NX_Q3KRB8

ARHGAP11B Protein expression data from MOPED and PaxDb:    About this image 
ARHGAP11B Protein Expression

REFSEQ proteins: NP_001034930.1  
ENSEMBL proteins: 
 ENSP00000457054   ENSP00000392760  
Reactome Protein details: Q3KRB8
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Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

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

ARHGAP11B 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

ARHGAP11B for domains           About GeneDecksing

2 InterPro domains/families:
 IPR008936 Rho_GTPase_activation_prot
 IPR000198 RhoGAP_dom

Graphical View of Domain Structure for InterPro Entry Q3KRB8

ProtoNet protein and cluster: Q3KRB8

1 Blocks protein family: IPB000198 RhoGAP domain

UniProtKB/Swiss-Prot: RHGBB_HUMAN, Q3KRB8
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, inGenious Targeting Laboratory,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

     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--
     
ARHGAP11B for ontologies           About GeneDecksing


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(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 ARHGAP11B
    Signaling by Rho GTPases
Signal Transduction
Rho GTPase cycle



ARHGAP11B for pathways           About GeneDecksing

Interactions:

    Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ARHGAP11B

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--

ARHGAP11B 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
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Browse Tocris compounds for ARHGAP11B
Search CenterWatch for drugs/clinical trials and news about ARHGAP11B / RHGBB 

(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,
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About This Section

REFSEQ mRNAs for ARHGAP11B gene: 
NM_001039841.1  

Unigene Cluster for ARHGAP11B:

Rho GTPase activating protein 11B
Hs.659621  [show with all ESTs]
Unigene Representative Sequence: BC071990
9 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000567449(uc010azu.1) ENST00000564902(uc010azv.1) ENST00000563110(uc001zet.1 uc001zeu.3)
ENST00000428041 ENST00000566362 ENST00000568574 ENST00000566548 ENST00000569416
ENST00000562954(uc001zev.3 uc021sht.1 uc021shu.1)

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Additional cDNA sequence: 

AK310319.1 BC071990.1 BC105788.1 

7 DOTS entries:

DT.102832216  DT.40282285  DT.121033551  DT.40128946  DT.121033548  DT.85104163  DT.95375483 

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

ARHGAP11B expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: AAAAGATGTC
ARHGAP11B Expression
About this image
See ARHGAP11B Protein Expression from SPIRE MOPED and PaxDB
SOURCE GeneReport for Unigene cluster: Hs.659621
    SABiosciences Custom PCR Arrays for ARHGAP11B

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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 animals.

Orthologs for ARHGAP11B gene from 4/14 species (see all 14)    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
chicken
(Gallus gallus)
Aves ARHGAP406
ARHGAP11A6
Uncharacterized protein
6(a)
31(a)
possible ortholog
1 ↔ many
Un(6089373-6095158)
5(32938888-32946851)
lizard
(Anolis carolinensis)
Reptilia --
--
14(a)
1 → many
1(32797942-32815043)
zebrafish
(Danio rerio)
Actinopterygii arhgap11a6
zgc:1533456
zgc:153345
14(a)
10(a)
1 ↔ many
possible ortholog
17(734497-755525)
10(34422004-34431697)
honey bee
(Apis mellifera)
Insecta --
--
8(a)
1 → many
GroupUn.960(669-4348)


ENSEMBL Gene Tree for ARHGAP11B (if available)
TreeFam Gene Tree for ARHGAP11B (if available) 

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
Paralogs for ARHGAP11B gene
ARHGAP362  ARHGAP62  STARD132  ARHGAP402  ARHGAP182  ARHGAP11A2  DLC12  ARHGAP282  
STARD82  
1 SIMAP similar gene for ARHGAP11B using alignment to 1 protein entry:     RHGBB_HUMAN:
ARHGAP11A

ARHGAP11B for paralogs           About GeneDecksing


1 Pseudogenes.org Pseudogene for ARHGAP11B
PGOHUM00000258954


(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

10/176 NCBI SNPs in ARHGAP11B are shown (see all 176    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 15 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs9005961,2
A--30916892(+) TACACT/CGTTTC 1 -- us2k11Minor allele frequency- C:0.00NA 2
rs1891075681,2
--30916907(+) TAAAAC/TTGATG 1 -- us2k10--------
rs1449051111,2
--30917242(+) CAACAC/TATTTA 1 -- us2k10--------
rs1490279191,2
--30917747(+) GCCACC/GTCCCG 1 -- us2k10--------
rs1489281591,2
--30917851(+) GTCCCC/GCAAAG 1 -- us2k10--------
rs18720911,2
C,F,A,H--30917889(+) ACCAAA/GGGCCG 1 -- us2k14Minor allele frequency- G:0.40NA 10
rs1480389801,2
C--30917909(+) TTACT-/AAAAAT 1 -- us2k10--------
rs665373521,2
C,F--30917948(-) CCCAGT/ATGAGA 1 -- us2k12Minor allele frequency- A:0.50NA WA 4
rs38338221,2
C--30917961(+) CCGTA-/AGAACG 1 -- us2k11Minor allele frequency- A:0.50NA 2
rs1921429201,2
--30917966(+) AGAACA/GGTTTC 1 -- us2k10--------

HapMap Linkage Disequilibrium report for ARHGAP11B (30916697 - 31060329 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 10 variations for ARHGAP11B
     9 CNVs: 66761 4887 3955 87581 3074 32014 9262 87582 66762
     1 Inversion: 37164

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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

ARHGAP11B for disorders           About GeneDecksing

1 disease for ARHGAP11B:    About MalaCards
exophthalmos


Export disorders for ARHGAP11B 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 ARHGAP11B gene integrated from 9 sources:
(articles sorted by number of sources associating them with ARHGAP11B)
    Utopia: connect your pdf to the dynamic
world of online information

  1. A 3-Mb map of a large segmental duplication overlapping the alpha7- nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. (PubMed id 11829490)1, 3 Riley B.... Makoff A. (2002)
  2. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
  3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)
  4. Generation and analysis of 280,000 human expressed sequence tags. (PubMed id 8889549)1 Hillier L.D....Marra M. (1996)

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

  Query String
PubMed
OMIM
NCBI Bookshelf
  (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: 89839 HGNC: 15782 Ensembl:ENSG00000187951 euGenes: HUgn89839 ECgene: ARHGAP11B
H-InvDB: ARHGAP11B

(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 ARHGAP11B 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 ARHGAP11B gene:
Search GeneIP for patents involving ARHGAP11B

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, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
Advanced Cell Diagnostics, Animal models from inGenious Targeting Laboratory)
About This Section

 
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GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013 , 14 May 2013

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VWF
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von Willebrand factor
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