Gene Gene information from NCBI Gene database.
Entrez ID 4893
Gene name NRAS proto-oncogene, GTPase
Gene symbol NRAS
Synonyms (NCBI Gene)
ALPS4CMNSKRASN-rasNCMSNRAS1NS6
Chromosome 1
Chromosome location 1p13.2
Summary This is an N-ras oncogene encoding a membrane protein that shuttles between the Golgi apparatus and the plasma membrane. This shuttling is regulated through palmitoylation and depalmitoylation by the ZDHHC9-GOLGA7 complex. The encoded protein, which has i
SNPs SNP information provided by dbSNP.
19
SNP ID Visualize variation Clinical significance Consequence
rs11554290 T>A,C,G Pathogenic, likely-pathogenic Missense variant, coding sequence variant
rs121434595 C>A,G,T Likely-pathogenic, pathogenic Missense variant, coding sequence variant
rs121434596 C>A,G,T Likely-pathogenic, pathogenic Missense variant, coding sequence variant
rs121913237 C>A,G,T Likely-pathogenic, pathogenic Missense variant, coding sequence variant
rs121913248 C>G,T Likely-pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
1606
miRTarBase ID miRNA Experiments Reference
MIRT003836 hsa-let-7b-5p ImmunohistochemistryqRT-PCR 19966857
MIRT001854 hsa-let-7a-5p Luciferase reporter assayMicroarray 15766527
MIRT004531 hsa-let-7c-5p MicroarrayNorthern blotqRT-PCRWestern blot 15766527
MIRT003903 hsa-miR-20a-5p Western blot 19110058
MIRT001854 hsa-let-7a-5p Western blot 19110058
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
AR Repression 16281084
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane TAS
GO:0000165 Process MAPK cascade IEA
GO:0000165 Process MAPK cascade TAS
GO:0000166 Function Nucleotide binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
164790 7989 ENSG00000213281
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P01111
Protein name GTPase NRas (EC 3.6.5.2) (Transforming protein N-Ras)
Protein function Ras proteins bind GDP/GTP and possess intrinsic GTPase activity.
PDB 2N9C , 3CON , 5UHV , 6E6H , 6MPP , 6ULI , 6ULK , 6ULN , 6ULR , 6UON , 6WGH , 6ZIO , 6ZIR , 6ZIZ , 7F68 , 7OW3 , 7OW4 , 7OW5 , 7OW6 , 7PB2 , 8TBI , 8VM2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 5 165 Ras family Domain
Sequence
Sequence length 189
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
70
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Acute megakaryoblastic leukemia in down syndrome Likely pathogenic; Pathogenic rs121434596 RCV001293767
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Acute myeloid leukemia Likely pathogenic; Pathogenic rs121434595, rs121434596 RCV000438070
RCV005887522
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Acute myeloid leukemia with NPM1 somatic mutations Likely pathogenic; Pathogenic rs121434596 RCV006253597
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Anemia Likely pathogenic rs1570874751 RCV001003789
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Alveolar rhabdomyosarcoma Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atypical teratoid rhabdoid tumor Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIO-FACIO-CUTANEOUS SYNDROME Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Abnormal dermatoglyphic pattern Abnormal dermatoglyphic pattern HPO_DG
★☆☆☆☆
Found in Text Mining only
Absence of septum pellucidum Absence Of Septum Pellucidum HPO_DG
★☆☆☆☆
Found in Text Mining only
Absent eyebrow Absent eyebrow HPO_DG
★☆☆☆☆
Found in Text Mining only
Accessory nipple Accessory Nipple HPO_DG
★☆☆☆☆
Found in Text Mining only
Achondroplasia Achondroplasia Pubtator 30355600 Associate
★☆☆☆☆
Found in Text Mining only
Acoustic Neuroma Acoustic Neuroma BEFREE 23224067
★☆☆☆☆
Found in Text Mining only
Acquired cubitus valgus Cubitus valgus HPO_DG
★☆☆☆☆
Found in Text Mining only
Acquired Kyphoscoliosis Acquired Kyphoscoliosis HPO_DG
★☆☆☆☆
Found in Text Mining only
Acquired porencephaly Acquired Porencephaly HPO_DG
★☆☆☆☆
Found in Text Mining only
Acral Lentiginous Malignant Melanoma Acral Lentiginous Malignant Melanoma BEFREE 26709572, 29512974
★☆☆☆☆
Found in Text Mining only