PanelApp
  1. Genes and Genomic Entities
  2. NRAS

NRAS

NRAS proto-oncogene, GTPase
OMIM: 164790, ClinGen, DECIPHER

17 panels

Panel Reviews Mode of inheritance Details
17 panels

Red NRAS in Haematological malignancies


Level 2: Cancer susceptibility
Version 0.148

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Other
Phenotypes
  • Noonan syndrome 6, MIM# 613224

Green NRAS in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.35

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green NRAS in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.5

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green NRAS in Macrocephaly_Megalencephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.8

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green NRAS in Mendeliome


Version 2.590

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Noonan syndrome 6, MIM# 613224

Green NRAS in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 1.2

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green NRAS in Rasopathy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Noonan syndrome 6, MIM# 613224

Green NRAS in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 1.25

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green NRAS in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.145

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Noonan syndrome 6, MIM# 613224

Red NRAS in Vascular Malformations_Germline


Level 2: Cardiovascular disorders
Version 2.1

Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  1 review Other
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Kaposiform lymphangiomatosis
    • Sporadic vascular malformation
    Tags
    • somatic

    Green NRAS in Lymphoedema

    Level 3: Lymphatic Disorders
    Level 2: Cardiovascular disorders
    Version 1.0

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  0 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Noonan syndrome 6 613224

    Green NRAS in Vascular Malformations_Somatic


    Level 2: Cardiovascular disorders
    Version 2.0

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  1 review Other
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Kaposiform lymphangiomatosis
    • Sporadic vascular malformation
    Tags
    • somatic

    Green NRAS in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 1.359

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • South West GLH
    • NHS GMS
    • Expert List
    • London South GLH
    Phenotypes
    • Noonan syndrome 6, MIM# 613224

    Green NRAS in Mosaic skin disorders


    Level 2: Dermatological disorders
    Version 2.0

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • NHS GMS
    Phenotypes
    • Noonan syndrome
    • Melanocytic naevi
    • Congenital melanocytic naevus syndrome
    Tags
    • somatic

    Green NRAS in Growth failure


    Version 2.28

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Noonan syndrome 6, MIM# 613224

    Green NRAS in Fetal anomalies


    Version 2.81

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Noonan syndrome 6, MIM# 613224

    Green NRAS in Autoimmune Lymphoproliferative Syndrome


    Level 2: Immunological disorders
    Version 2.0

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • autoimmune lymphoproliferative syndrome type 4 MONDO:0013767