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RASD2 (RASD family member 2)

Identity

Alias (NCBI)Rhes
TEM2
HGNC (Hugo) RASD2
HGNC Alias symbTEM2
Rhes
MGC:4834
HGNC Alias nametumor endothelial marker 2
 Ras homolog enriched in striatum
HGNC Previous nameRASD family, member 2
LocusID (NCBI) 23551
Atlas_Id 43449
Location 22q12.3  [Link to chromosome band 22q12]
Location_base_pair Starts at 35540831 and ends at 35553998 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 



External links

 

Nomenclature
HGNC (Hugo)RASD2   18229
Cards
Entrez_Gene (NCBI)RASD2    RASD family member 2
AliasesRhes; TEM2
GeneCards (Weizmann)RASD2
Ensembl hg19 (Hinxton)ENSG00000100302 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000100302 [Gene_View]  ENSG00000100302 [Sequence]  chr22:35540831-35553998 [Contig_View]  RASD2 [Vega]
ICGC DataPortalENSG00000100302
TCGA cBioPortalRASD2
AceView (NCBI)RASD2
Genatlas (Paris)RASD2
SOURCE (Princeton)RASD2
Genetics Home Reference (NIH)RASD2
Genomic and cartography
GoldenPath hg38 (UCSC)RASD2  -     chr22:35540831-35553998 +  22q12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RASD2  -     22q12.3   [Description]    (hg19-Feb_2009)
GoldenPathRASD2 - 22q12.3 [CytoView hg19]  RASD2 - 22q12.3 [CytoView hg38]
ImmunoBaseENSG00000100302
Genome Data Viewer NCBIRASD2 [Mapview hg19]  
OMIM612842   
Gene and transcription
Genbank (Entrez)AF279143 AL831936 BC013419 CR456477
RefSeq transcript (Entrez)NM_001366725 NM_001376515 NM_001376516 NM_014310
Consensus coding sequences : CCDS (NCBI)RASD2
Gene ExpressionRASD2 [ NCBI-GEO ]   RASD2 [ EBI - ARRAY_EXPRESS ]   RASD2 [ SEEK ]   RASD2 [ MEM ]
Gene Expression Viewer (FireBrowse)RASD2 [ Firebrowse - Broad ]
GenevisibleExpression of RASD2 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)23551
GTEX Portal (Tissue expression)RASD2
Human Protein AtlasENSG00000100302-RASD2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96D21   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96D21  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96D21
PhosPhoSitePlusQ96D21
Domaine pattern : Prosite (Expaxy)RAS (PS51421)   
Domains : Interpro (EBI)P-loop_NTPase    Small_GTP-bd_dom    Small_GTPase    Small_GTPase_Ras-type   
Domain families : Pfam (Sanger)Ras (PF00071)   
Domain families : Pfam (NCBI)pfam00071   
Conserved Domain (NCBI)RASD2
SuperfamilyQ96D21
AlphaFold pdb e-kbQ96D21   
Human Protein Atlas [tissue]ENSG00000100302-RASD2 [tissue]
HPRD15210
Protein Interaction databases
DIP (DOE-UCLA)Q96D21
IntAct (EBI)Q96D21
BioGRIDRASD2
STRING (EMBL)RASD2
ZODIACRASD2
Ontologies - Pathways
QuickGOQ96D21
Ontology : AmiGOGTPase activity  GTP binding  plasma membrane  signal transduction  locomotory behavior  negative regulation of protein ubiquitination  ubiquitin conjugating enzyme binding  G-protein beta-subunit binding  positive regulation of protein sumoylation  phosphatidylinositol 3-kinase binding  regulation of cAMP-mediated signaling  positive regulation of protein kinase B signaling  
Ontology : EGO-EBIGTPase activity  GTP binding  plasma membrane  signal transduction  locomotory behavior  negative regulation of protein ubiquitination  ubiquitin conjugating enzyme binding  G-protein beta-subunit binding  positive regulation of protein sumoylation  phosphatidylinositol 3-kinase binding  regulation of cAMP-mediated signaling  positive regulation of protein kinase B signaling  
NDEx NetworkRASD2
Atlas of Cancer Signalling NetworkRASD2
Wikipedia pathwaysRASD2
Orthology - Evolution
OrthoDB23551
GeneTree (enSembl)ENSG00000100302
Phylogenetic Trees/Animal Genes : TreeFamRASD2
Homologs : HomoloGeneRASD2
Homology/Alignments : Family Browser (UCSC)RASD2
Gene fusions - Rearrangements
Fusion : QuiverRASD2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerRASD2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)RASD2
dbVarRASD2
ClinVarRASD2
MonarchRASD2
1000_GenomesRASD2 
Exome Variant ServerRASD2
GNOMAD BrowserENSG00000100302
Varsome BrowserRASD2
ACMGRASD2 variants
VarityQ96D21
Genomic Variants (DGV)RASD2 [DGVbeta]
DECIPHERRASD2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisRASD2 
Mutations
ICGC Data PortalRASD2 
TCGA Data PortalRASD2 
Broad Tumor PortalRASD2
OASIS PortalRASD2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICRASD2  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DRASD2
Mutations and Diseases : HGMDRASD2
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaRASD2
DgiDB (Drug Gene Interaction Database)RASD2
DoCM (Curated mutations)RASD2
CIViC (Clinical Interpretations of Variants in Cancer)RASD2
Cancer3DRASD2
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM612842   
Orphanet
DisGeNETRASD2
MedgenRASD2
Genetic Testing Registry RASD2
NextProtQ96D21 [Medical]
GENETestsRASD2
Target ValidationRASD2
Huge Navigator RASD2 [HugePedia]
ClinGenRASD2
Clinical trials, drugs, therapy
MyCancerGenomeRASD2
Protein Interactions : CTDRASD2
Pharm GKB GenePA34237
PharosQ96D21
Clinical trialRASD2
Miscellaneous
canSAR (ICR)RASD2
HarmonizomeRASD2
DataMed IndexRASD2
Probes
Litterature
PubMed29 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXRASD2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:28:19 CEST 2021

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