This Panel is marked as Retired
TCGA_PANCAN_2018
Gene: NRAS
NRAS (NRAS proto-oncogene, GTPase)
EnsemblGeneIds (GRCh38): ENSG00000213281
EnsemblGeneIds (GRCh37): ENSG00000213281
OMIM: 164790, Gene2Phenotype
NRAS is in 18 panels
EnsemblGeneIds (GRCh38): ENSG00000213281
EnsemblGeneIds (GRCh37): ENSG00000213281
OMIM: 164790, Gene2Phenotype
NRAS is in 18 panels
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Details
- Mode of Inheritance
- Other
- Sources
-
- TCGA_PANCAN_2018
- Phenotypes
-
- Congenital giant melanocytic nevus
- Rasopathy
- RAS-associated autoimmune leukoproliferative disorder
- NA
- Noonan syndrome 6
- Epidermal nevus
- OMIM
- 164790
- Clinvar variants
- Variants in NRAS
- Penetrance
- None
- Panels with this gene
-
- Rasopathy
- Calcium and Phosphate disorders
- Cardiomyopathy_Paediatric
- Lymphoedema_syndromic
- Vasculitis
- Hydrops fetalis
- Intellectual disability syndromic and non-syndromic
- Cancer Predisposition_Paediatric
- Vascular Malformations_Germline
- Macrocephaly_Megalencephaly
- Vascular Malformations_Somatic
- Fetal anomalies
- Congenital Heart Defect
- Autoimmune Lymphoproliferative Syndrome
- Mosaic skin disorders
- Mendeliome
- Callosome
- Growth failure
History Filter Activity
8 Jan 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Lavinia Gordon (UMCCR)gene: NRAS was added gene: NRAS was added to TCGA_PANCAN_2018. Sources: TCGA_PANCAN_2018 Mode of inheritance for gene: NRAS was set to Other Phenotypes for gene: NRAS were set to Congenital giant melanocytic nevus; Rasopathy; RAS-associated autoimmune leukoproliferative disorder; NA; Noonan syndrome 6; Epidermal nevus