Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23551
Gene name Gene Name - the full gene name approved by the HGNC.
RASD family member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RASD2
Synonyms (NCBI Gene) Gene synonyms aliases
Rhes, TEM2
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the prote
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT448097 hsa-miR-3928-3p PAR-CLIP 22100165
MIRT448095 hsa-miR-4804-3p PAR-CLIP 22100165
MIRT448096 hsa-miR-4720-3p PAR-CLIP 22100165
MIRT448094 hsa-miR-3915 PAR-CLIP 22100165
MIRT448093 hsa-miR-1224-5p PAR-CLIP 22100165
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003924 Function GTPase activity NAS 11976265
GO:0005525 Function GTP binding IEA
GO:0005886 Component Plasma membrane ISS
GO:0007165 Process Signal transduction IEA
GO:0007626 Process Locomotory behavior ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612842 18229 ENSG00000100302
Protein
UniProt ID Q96D21
Protein name GTP-binding protein Rhes (Ras homolog enriched in striatum) (Tumor endothelial marker 2)
Protein function GTPase signaling protein that binds to and hydrolyzes GTP. Regulates signaling pathways involving G-proteins-coupled receptor and heterotrimeric proteins such as GNB1, GNB2 and GNB3. May be involved in selected striatal competencies, mainly loco
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 21 191 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Pancreatic endocrine cells (islets of Langerhans). {ECO:0000269|PubMed:11976265}.
Sequence
Sequence length 266
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
18571626, 23555897
Associations from Text Mining
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 30886340
Drug Related Side Effects and Adverse Reactions Associate 21779398
Epilepsy Associate 37192718
Glioma Associate 37192718
Huntington Disease Associate 21779398
Neoplasms Associate 19440709