NRAS Protooncogene, GTPase

Alternative Names

  • NRAS
  • Neuroblastoma Ras Viral Oncogene Homolog
  • Oncogene NRAS
  • NRAS1
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OMIM Number

164790

NCBI Gene ID

4893

Uniprot ID

P01111

Length

12,303 bases

No. of Exons

7

No. of isoforms

1

Protein Name

GTPase NRas

Molecular Mass

21229 Da

Amino Acid Count

189

Genomic Location

chr1:114,704,468-114,716,770

Gene Map Locus
1p13.2

Description

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 intrinsic GTPase activity, is activated by a guanine nucleotide-exchange factor and inactivated by a GTPase activating protein. Mutations in this gene have been associated with somatic rectal cancer, follicular thyroid cancer, autoimmune lymphoproliferative syndrome, Noonan syndrome, and juvenile myelomonocytic leukemia. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_002524.5:c.181C>ALebanonNC_000001.11:g.114713909G>TDrug Response, Likely Pathogenic, Pathogenic, Uncertain SignificanceLikely PathogenicThyroid Carcinoma, PapillaryNG_007572.1:g.7986C>A; NM_002524.5:c.181C>A; NP_002515.1:p.Gln61Lys12191325473058
NM_002524.5:c.182A>GLebanonNC_000001.11:g.114713908T>CLikely Pathogenic, PathogenicNG_007572.1:g.7987A>G; NM_002524.5:c.182A>G; NP_002515.1:p.Gln61Arg1155429013900
NM_002524.5:c.34G>ALebanonNC_000001.11:g.114716127C>TLikely Pathogenic, PathogenicLikely PathogenicThyroid Carcinoma, PapillaryNG_007572.1:g.5768G>A; NM_002524.5:c.34G>A; NP_002515.1:p.Gly12Ser121913250177778
NM_002524.5:c.38G>ALebanonNC_000001.11:g.114716123C>TLikely Pathogenic, PathogenicLikely PathogenicThyroid Carcinoma, PapillaryNG_007572.1:g.5772G>A; NM_002524.5:c.38G>A; NP_002515.1:p.Gly13Asp12143459613901

Other Reports

Arab

Al-Shamsi et al. 2021 delineated the somatic mutational spectrum and frequency in Arab women with breast cancer. 78 women mostly with stage 3 or 4 breast cancer exhibited mutations and mutation rates in the following genes: TP53, 23.1%; ATM, 2.6%; IDH1, 2.6%; IDH2, 3.8%; PTEN, 7.7%; PIK3CA, 15.4%; APC, 7.7%; NPM1, 2.5%; MPL, 1.3%; JAK2, 2.5%; KIT, 7.7%; KRAS, 3.8%; and NRAS, 3.8%

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