Human Gene ARHGAP33 (ENST00000314737.9) from GENCODE V44
  Description: Homo sapiens Rho GTPase activating protein 33 (ARHGAP33), transcript variant 1, mRNA. (from RefSeq NM_052948)
RefSeq Summary (NM_052948): This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Alternative splice variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Feb 2010].
Gencode Transcript: ENST00000314737.9
Gencode Gene: ENSG00000004777.19
Transcript (Including UTRs)
   Position: hg38 chr19:35,775,575-35,788,822 Size: 13,248 Total Exon Count: 21 Strand: +
Coding Region
   Position: hg38 chr19:35,775,659-35,788,429 Size: 12,771 Coding Exon Count: 21 

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RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr19:35,775,575-35,788,822)mRNA (may differ from genome)Protein (1126 aa)
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HGNCHPRDLynxMGIneXtProtOMIM
PubMedReactomeUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: RHG33_HUMAN
DESCRIPTION: RecName: Full=Rho GTPase-activating protein 33; AltName: Full=Rho-type GTPase-activating protein 33; AltName: Full=Sorting nexin-26; AltName: Full=Tc10/CDC42 GTPase-activating protein;
FUNCTION: May be involved in several stages of intracellular trafficking. Could play an important role in the regulation of glucose transport by insulin. May act as a downstream effector of RHOQ/TC10 in the regulation of insulin-stimulated glucose transport (By similarity).
SUBUNIT: Specifically interacts with CDC42 and RHOQ/TC10 through its Rho-GAP domain (By similarity). Interacts with NEK6.
INTERACTION: P06241:FYN; NbExp=2; IntAct=EBI-1210010, EBI-515315;
SIMILARITY: Belongs to the PX domain-containing GAP family.
SIMILARITY: Contains 1 PX (phox homology) domain.
SIMILARITY: Contains 1 Rho-GAP domain.
SIMILARITY: Contains 1 SH3 domain.
SEQUENCE CAUTION: Sequence=AAB81198.1; Type=Erroneous gene model prediction;

-  Primer design for this transcript
 

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Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
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To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: ARHGAP33
Diseases sorted by gene-association score: noma (27)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 34.00 RPKM in Testis
Total median expression: 532.04 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -34.1084-0.406 Picture PostScript Text
3' UTR -121.30393-0.309 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR001683 - Phox
IPR008936 - Rho_GTPase_activation_prot
IPR000198 - RhoGAP_dom
IPR011511 - SH3_2
IPR001452 - SH3_domain

Pfam Domains:
PF00620 - RhoGAP domain
PF07653 - Variant SH3 domain

ModBase Predicted Comparative 3D Structure on O14559
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
MGIRGD    
Protein SequenceProtein Sequence    
AlignmentAlignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005096 GTPase activator activity
GO:0005515 protein binding
GO:0019901 protein kinase binding
GO:0035091 phosphatidylinositol binding

Biological Process:
GO:0007165 signal transduction
GO:0007264 small GTPase mediated signal transduction
GO:0009636 response to toxic substance
GO:0015031 protein transport
GO:0043547 positive regulation of GTPase activity
GO:0051056 regulation of small GTPase mediated signal transduction
GO:0061001 regulation of dendritic spine morphogenesis

Cellular Component:
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005938 cell cortex
GO:0015629 actin cytoskeleton
GO:0032991 macromolecular complex
GO:0043197 dendritic spine


-  Descriptions from all associated GenBank mRNAs
  AK127255 - Homo sapiens cDNA FLJ45322 fis, clone BRHIP3006294, moderately similar to Mus musculus Cdc42 GTPase-activating protein (Cdgap).
AK096338 - Homo sapiens cDNA FLJ39019 fis, clone NT2RP7002738, highly similar to Homo sapiens sorting nexin 26 (SNX26), mRNA.
BC128586 - Homo sapiens sorting nexin 26, mRNA (cDNA clone MGC:157744 IMAGE:40129027), complete cds.
AL137579 - Homo sapiens mRNA; cDNA DKFZp434A1010 (from clone DKFZp434A1010).
AY044864 - Homo sapiens sorting nexin 26 (SNX26) mRNA, complete cds.
JD052325 - Sequence 33349 from Patent EP1572962.
JD169851 - Sequence 150875 from Patent EP1572962.
BC014084 - Homo sapiens sorting nexin 26, mRNA (cDNA clone IMAGE:4300179), partial cds.
JD466344 - Sequence 447368 from Patent EP1572962.
JD163796 - Sequence 144820 from Patent EP1572962.
JD158335 - Sequence 139359 from Patent EP1572962.
JD544819 - Sequence 525843 from Patent EP1572962.
JD130363 - Sequence 111387 from Patent EP1572962.
JD094364 - Sequence 75388 from Patent EP1572962.
JD479397 - Sequence 460421 from Patent EP1572962.
JD479398 - Sequence 460422 from Patent EP1572962.
JD420303 - Sequence 401327 from Patent EP1572962.
JD418465 - Sequence 399489 from Patent EP1572962.
JD123210 - Sequence 104234 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein O14559 (Reactome details) participates in the following event(s):

R-HSA-194922 GAPs inactivate Rho GTPase:GTP by hydrolysis
R-HSA-194840 Rho GTPase cycle
R-HSA-194315 Signaling by Rho GTPases
R-HSA-162582 Signal Transduction

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000314737.1, ENST00000314737.2, ENST00000314737.3, ENST00000314737.4, ENST00000314737.5, ENST00000314737.6, ENST00000314737.7, ENST00000314737.8, NM_052948, O14552, O14559, O14560, Q6ZSP6, Q96CP3, Q9NT23, RHG33_HUMAN, SNX26, TCGAP, uc002obs.1, uc002obs.2, uc002obs.3
UCSC ID: ENST00000314737.9
RefSeq Accession: NM_052948
Protein: O14559 (aka RHG33_HUMAN)
CCDS: CCDS12477.1

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.