Nras (GeneID: 18176) | Mus musculus
Description: neuroblastoma ras oncogene [Source:MGI Symbol;Acc:MGI:97376]
Synonyms: AV095280, N-ras
Other ID(s): MGI:97376, ENSMUSG00000027852
Protein Accession Numbers: XP_006501181, XP_006501186, XP_006501183, NP_035067, XP_006501185, XP_006501182, NP_001355567, XP_006501184
Statistics: ClinVar(82) gnomAD(110) COSMIC(4066) PTM(13)
ClinVar Pathogenicity of Variations help

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000369535 You are here now! NP_002515 You are here now!


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00071 Ras Ras family 5-165 CL0023 P-loop_NTPase Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Malignant Neoplasms Neoplasms ; 0.42 0.69
Rectal Carcinoma Neoplasms ; Digestive System Diseases ; 0.42 0.69
Malignant neoplasm of thyroid N/A 0.42 0.69
Non-Small Cell Lung Carcinoma Neoplasms ; Respiratory Tract Diseases ; 0.42 0.69
Hypertrophic Cardiomyopathy Cardiovascular Diseases ; 0.42 0.69
Charcot-Marie-Tooth Disease Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Colorectal Carcinoma Neoplasms ; Digestive System Diseases ; 0.42 0.69
Colorectal Neoplasms Neoplasms ; Digestive System Diseases ; 0.42 0.69
Cytopenia N/A 0.42 0.69
Hydrocephalus Nervous System Diseases ; 0.42 0.69
Hydrops Fetalis Female Urogenital Diseases and Pregnancy Complications ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Immune System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.42 0.69
leukemia Neoplasms ; 0.42 0.69
Leukemia, Myelocytic, Acute Neoplasms ; 0.42 0.69
Myeloid Leukemia, Chronic Neoplasms ; Hemic and Lymphatic Diseases ; 0.42 0.69
Leukemia, Myelomonocytic, Chronic Neoplasms ; Hemic and Lymphatic Diseases ; 0.42 0.69
Acute Promyelocytic Leukemia Neoplasms ; 0.42 0.69
Leukocytosis Hemic and Lymphatic Diseases ; Pathological Conditions, Signs and Symptoms ; 0.42 0.69
Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.42 0.69
melanoma Neoplasms ; 0.42 0.69
Multiple Myeloma Neoplasms ; Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.42 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.42 0.69
Myelomonocytic leukemia N/A 0.42 0.69
Neoplasms, Experimental Neoplasms ; 0.42 0.69
Neuroblastoma Neoplasms ; 0.42 0.69
Noonan Syndrome Musculoskeletal Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.42 0.69
Rectal Neoplasms Neoplasms ; Digestive System Diseases ; 0.42 0.69
Splenomegaly Pathological Conditions, Signs and Symptoms ; 0.42 0.69
Thyroid Neoplasm Neoplasms ; Endocrine System Diseases ; 0.42 0.69
Turner Syndrome, Male Musculoskeletal Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.42 0.69
B-Cell Lymphomas Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.42 0.69
Adenocarcinoma of rectum N/A 0.42 0.69
Cutaneous Melanoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.42 0.69
Pleocytosis Hemic and Lymphatic Diseases ; Pathological Conditions, Signs and Symptoms ; 0.42 0.69
Adenocarcinoma of lung (disorder) Neoplasms ; Respiratory Tract Diseases ; 0.42 0.69
Congenital anemia N/A 0.42 0.69
Follicular thyroid carcinoma Neoplasms ; 0.42 0.69
Neurofibrosarcoma Neoplasms ; Nervous System Diseases ; 0.42 0.69
Epithelioid and spindle cell nevus Neoplasms ; 0.42 0.69
Papillary thyroid carcinoma Neoplasms ; Endocrine System Diseases ; 0.42 0.69
Organoid Nevus Phakomatosis Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Gastric Adenocarcinoma N/A 0.42 0.69
NEVUS, EPIDERMAL (disorder) Neoplasms ; 0.42 0.69
Woolly hair nevus N/A 0.42 0.69
Nevus spilus N/A 0.42 0.69
Juvenile Myelomonocytic Leukemia Neoplasms ; Hemic and Lymphatic Diseases ; 0.42 0.69
Verrucous epidermal nevus Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Inflammatory linear verrucous epidermal nevus Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Epileptic encephalopathy N/A 0.42 0.69
Neurocutaneous melanosis Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.42 0.69
Thyroid carcinoma Neoplasms ; Endocrine System Diseases ; 0.42 0.69
Congenital melanocytic nevus N/A 0.42 0.69
Adenocarcinoma of large intestine N/A 0.42 0.69
Autoimmune Lymphoproliferative Syndrome Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Immune System Diseases ; 0.42 0.69
Colorectal Cancer Neoplasms ; Digestive System Diseases ; 0.42 0.69
Female Pseudo-Turner Syndrome Musculoskeletal Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.42 0.69
GIANT PIGMENTED HAIRY NEVUS Neoplasms ; Skin and Connective Tissue Diseases ; 0.42 0.69
Autoimmune Lymphoproliferative Syndrome Type 2B Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Immune System Diseases ; 0.42 0.69
Leukemia, Megakaryoblastic, of Down Syndrome Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.42 0.69
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER N/A 0.42 0.69
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Immune System Diseases ; 0.42 0.69
Noonan Syndrome 6 Musculoskeletal Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.42 0.69
Thyroid cancer, follicular Neoplasms ; 0.42 0.69
Linear Verrucous Epidermal Nevus Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.42 0.69
Nevus sebaceous Neoplasms ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.42 0.69
Nevus, Keratinocytic, Nonepidermolytic Neoplasms ; 0.42 0.69
THYROID CANCER, NONMEDULLARY, 2 N/A 0.42 0.69
NO RESULT FOUND
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