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RASD2 (RASD family member 2)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23551
Gene nameGene Name - the full gene name approved by the HGNC.
RASD family member 2
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
RASD2
SynonymsGene synonyms aliases
Rhes, TEM2
ChromosomeChromosome number
22
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q12.3
SummarySummary 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
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Sequence
Sequence length 266
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 18571626, 23555897

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