Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
22808
Gene name Gene Name - the full gene name approved by the HGNC.
Muscle RAS oncogene homolog
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MRAS
Synonyms (NCBI Gene) Gene synonyms aliases
M-RAs, NS11, R-RAS3, RRAS3
Disease Acronyms (UniProt) Disease acronyms from UniProt database
NS11
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the Ras family of small GTPases. These membrane-associated proteins function as signal transducers in multiple processes including cell growth and differentiation, and dysregulation of Ras signaling has been associated with m
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1560171992 G>C Likely-pathogenic Missense variant, intron variant, coding sequence variant
rs1576359216 G>T Pathogenic Intron variant, missense variant, coding sequence variant
rs1576387876 C>T Pathogenic, likely-pathogenic 5 prime UTR variant, coding sequence variant, missense variant
rs1576387885 A>G Pathogenic 5 prime UTR variant, coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT039529 hsa-miR-652-3p CLASH 23622248
MIRT473045 hsa-miR-2392 PAR-CLIP 23592263
MIRT473044 hsa-miR-3605-5p PAR-CLIP 23592263
MIRT473043 hsa-miR-185-5p PAR-CLIP 23592263
MIRT473042 hsa-miR-4306 PAR-CLIP 23592263
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 IBA 21873635
GO:0003924 Function GTPase activity IMP 28289718
GO:0005515 Function Protein binding IPI 25137548
GO:0005525 Function GTP binding IBA 21873635
GO:0005886 Component Plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608435 7227 ENSG00000158186
Protein
UniProt ID O14807
Protein name Ras-related protein M-Ras (EC 3.6.5.2) (Ras-related protein R-Ras3)
Protein function Signal transducer in the Ras-MAPK signaling pathway that regulates cell proliferation and survival (PubMed:16630891, PubMed:28289718, PubMed:35768504, PubMed:35830882, PubMed:35831509, PubMed:36175670). Core component of the SHOC2-MRAS-PP1c (SMP
PDB 7SD0 , 7TVF , 7TXH , 7UPI , 9B4R , 9B4T , 9C1A , 9C1B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 15 177 Ras family Domain
Tissue specificity TISSUE SPECIFICITY: Expression highly restricted to the brain and heart.
Sequence
Sequence length 208
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  MAPK signaling pathway
Ras signaling pathway
Rap1 signaling pathway
Phospholipase D signaling pathway
Mitophagy - animal
Autophagy - animal
Cellular senescence
Apelin signaling pathway
C-type lectin receptor signaling pathway
Regulation of actin cytoskeleton
Proteoglycans in cancer
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial septal defect Atrial Septal Defects rs137852951, rs137852953, rs137852955, rs267607106, rs104893900, rs104893901, rs104893903, rs606231358, rs606231359, rs137852683, rs606231360, rs104893907, rs104894073, rs1585703301, rs104894074
View all (25 more)
Brachydactyly Brachydactyly rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)
Cardiofaciocutaneous syndrome Cardio-facio-cutaneous syndrome rs121434497, rs121434498, rs121434499, rs267607230, rs121913530, rs104894359, rs104894360, rs104894366, rs104894361, rs104894362, rs121908594, rs121908595, rs121908596, rs121913348, rs180177034
View all (61 more)
Coronary artery disease CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1, Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 23202125, 21378990, 24262325, 28714975, 29212778
Unknown
Disease term Disease name Evidence References Source
Coronary heart disease Coronary heart disease 24262325, 21347282, 19198612, 21378990, 28869590 ClinVar
Ptosis Blepharoptosis, Ptosis ClinVar
Noonan Syndrome Noonan syndrome GenCC
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Abidi X linked mental retardation syndrome Associate 28737528
Atherosclerosis Associate 32495899
Breast Neoplasms Associate 22121046
Burkitt Lymphoma Associate 26325594
Carcinogenesis Associate 22121046, 27891760
Carcinoma Non Small Cell Lung Associate 33106373
Cardiomegaly Associate 28289718, 31638832
Cardiomyopathy Hypertrophic Associate 36734411, 37141804
Cardiovascular Diseases Associate 23738802, 31770223
Central Nervous System Diseases Associate 24148564