Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51655
Gene name Gene Name - the full gene name approved by the HGNC.
Ras related dexamethasone induced 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RASD1
Synonyms (NCBI Gene) Gene synonyms aliases
AGS1, DEXRAS1, MGC:26290
Disease Acronyms (UniProt) Disease acronyms from UniProt database
AGS1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the Ras superfamily of small GTPases and is induced by dexamethasone. The encoded protein is an activator of G-protein signaling and acts as a direct nucleotide exchange factor for Gi-Go proteins. This protein interacts with
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004439 hsa-miR-375 Luciferase reporter assay, Microarray, qRT-PCR 20978187
MIRT018256 hsa-miR-335-5p Microarray 18185580
MIRT492476 hsa-miR-139-3p PAR-CLIP 20371350
MIRT492475 hsa-miR-149-3p PAR-CLIP 20371350
MIRT492474 hsa-miR-4728-5p PAR-CLIP 20371350
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 IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
GO:0005525 Function GTP binding IEA
GO:0005634 Component Nucleus IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605550 15828 ENSG00000108551
Protein
UniProt ID Q9Y272
Protein name Dexamethasone-induced Ras-related protein 1 (Activator of G-protein signaling 1)
Protein function Small GTPase. Negatively regulates the transcription regulation activity of the APBB1/FE65-APP complex via its interaction with APBB1/FE65 (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 26 196 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in a variety of tissues including heart, cardiovascular tissues, brain, placenta, lung, liver, skeletal muscle, kidney, pancreas, gastrointestinal and reproductive tissues. {ECO:0000269|PubMed:10673050, ECO:0000269|PubMed:128
Sequence
Sequence length 281
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Circadian entrainment
Cushing syndrome
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 17013881
Unknown
Disease term Disease name Evidence References Source
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
ACTH Secreting Pituitary Adenoma Associate 28487882
Allergic Fungal Sinusitis Associate 29270391
Asthma Associate 36012391
Atrophy Associate 36130474
Breast Neoplasms Associate 33255991
Carcinoma Non Small Cell Lung Associate 34363324
Cardiomyopathy Hypertrophic Associate 38006610
Drug Related Side Effects and Adverse Reactions Associate 36130474
Graves Ophthalmopathy Associate 35896115
Hereditary Breast and Ovarian Cancer Syndrome Associate 36130474