CSF2 (GeneID: 471627) | Pan troglodytes
Description: colony stimulating factor 2 [Source:VGNC Symbol;Acc:VGNC:6847]
Synonyms:
Other ID(s): ENSPTRG00000017212
Protein Accession Numbers: XP_527005
Statistics: ClinVar(5) gnomAD(124) COSMIC(41) PTM(3)
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.
ENST00000296871 You are here now! NP_000749 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
PF01109 GM_CSF Granulocyte-macrophage colony-stimulating factor 18-139 CL0053 4H_Cytokine Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Agranulocytosis Hemic and Lymphatic Diseases ; 0.356 0.966
Amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Anemia Hemic and Lymphatic Diseases ; 0.356 0.966
Aplastic Anemia Hemic and Lymphatic Diseases ; 0.356 0.966
Rheumatoid Arthritis Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.356 0.966
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.356 0.966
Carcinoma Neoplasms ; 0.356 0.966
Colorectal Carcinoma Neoplasms ; Digestive System Diseases ; 0.356 0.966
Colorectal Neoplasms Neoplasms ; Digestive System Diseases ; 0.356 0.966
Diastematomyelia Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Drug toxicity Chemically-Induced Disorders ; 0.356 0.966
Eyelid Diseases Eye Diseases ; 0.356 0.966
Gastrointestinal Hemorrhage Digestive System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Heart failure Cardiovascular Diseases ; 0.356 0.966
Congestive heart failure Cardiovascular Diseases ; 0.356 0.966
Hematochezia Digestive System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Inflammation Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Left-Sided Heart Failure Cardiovascular Diseases ; 0.356 0.966
Leishmaniasis, Visceral Parasitic Diseases ; 0.356 0.966
Leukemia, Myelocytic, Acute Neoplasms ; 0.356 0.966
Liver neoplasms Neoplasms ; Digestive System Diseases ; 0.356 0.966
Reticulosarcoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Lymphoma, Mixed-Cell Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Lymphoma, Non-Hodgkin Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Lymphoma, Undifferentiated Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
melanoma Neoplasms ; 0.356 0.966
Multiple Myeloma Neoplasms ; Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Acute Myeloid Leukemia, M1 Neoplasms ; 0.356 0.966
Neural Tube Defects Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Neurenteric Cyst Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Neutropenia Hemic and Lymphatic Diseases ; 0.356 0.966
Pain Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Pustulosis of Palms and Soles Skin and Connective Tissue Diseases ; 0.356 0.966
Pneumonia Respiratory Tract Diseases ; 0.356 0.966
Lobar Pneumonia Respiratory Tract Diseases ; 0.356 0.966
Psoriasis Skin and Connective Tissue Diseases ; 0.356 0.966
Pulmonary Fibrosis Respiratory Tract Diseases ; 0.356 0.966
Schizophrenia Mental Disorders ; 0.356 0.966
Thrombocytopenia Hemic and Lymphatic Diseases ; 0.356 0.966
Thyroid Neoplasm Neoplasms ; Endocrine System Diseases ; 0.356 0.966
Adverse reaction to drug Chemically-Induced Disorders ; 0.356 0.966
Venous Thrombosis Cardiovascular Diseases ; 0.356 0.966
High Grade Lymphoma (neoplasm) Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Lymphoma, Intermediate-Grade Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Low Grade Lymphoma (neoplasm) Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Diffuse Mixed-Cell Lymphoma Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Lymphoma, Small Noncleaved-Cell Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Tethered Cord Syndrome Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Lymphoma, AIDS-Related Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Hamman-Rich syndrome Respiratory Tract Diseases ; 0.356 0.966
Deep Vein Thrombosis Cardiovascular Diseases ; 0.356 0.966
Thyroid Gland Follicular Adenoma Neoplasms ; Endocrine System Diseases ; 0.356 0.966
Muscle Weakness Musculoskeletal Diseases ; Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Iniencephaly Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Craniorachischisis Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Hypoplastic anemia Hemic and Lymphatic Diseases ; 0.356 0.966
Anaplastic carcinoma Neoplasms ; 0.356 0.966
Carcinoma, Spindle-Cell Neoplasms ; 0.356 0.966
Undifferentiated carcinoma Neoplasms ; 0.356 0.966
Carcinomatosis Neoplasms ; 0.356 0.966
Sarcoma, Epithelioid Neoplasms ; 0.356 0.966
Sarcoma, Spindle Cell Neoplasms ; 0.356 0.966
Hysterical amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Temporary Amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Pain, Burning Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Ache Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Radiating pain Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Heart Failure, Right-Sided Cardiovascular Diseases ; 0.356 0.966
Dissociative Amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Residual Cancer Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Neoplasm, Residual Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Global Amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Exencephaly Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Inflammatory disease of mucous membrane Digestive System Diseases ; Stomatognathic Diseases ; 0.356 0.966
Spinal Cord Myelodysplasia Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Malignant neoplasm of liver Neoplasms ; Digestive System Diseases ; 0.356 0.966
Juvenile Myelomonocytic Leukemia Neoplasms ; Hemic and Lymphatic Diseases ; 0.356 0.966
Non-alcoholic Fatty Liver Disease Digestive System Diseases ; 0.356 0.966
Pain, Splitting Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Pain, Crushing Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Residual Tumor Neoplasms ; Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Thyroid carcinoma Neoplasms ; Endocrine System Diseases ; 0.356 0.966
Breast Carcinoma Neoplasms ; Skin and Connective Tissue Diseases ; 0.356 0.966
Acrania Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.356 0.966
Tactile Amnesia Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Amnestic State Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.356 0.966
Pain, Migratory Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Suffering, Physical Pathological Conditions, Signs and Symptoms ; 0.356 0.966
Experimental Lung Inflammation Respiratory Tract Diseases ; 0.356 0.966
Mammary Neoplasms, Human Neoplasms ; Skin and Connective Tissue Diseases ; 0.356 0.966
Sarcoma Neoplasms ; 0.356 0.966
Mammary Neoplasms Neoplasms ; Skin and Connective Tissue Diseases ; 0.356 0.966
Colorectal Cancer Neoplasms ; Digestive System Diseases ; 0.356 0.966
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.356 0.966
Myocardial Failure Cardiovascular Diseases ; 0.356 0.966
Heart Decompensation Cardiovascular Diseases ; 0.356 0.966
Bone Marrow failure syndromes Hemic and Lymphatic Diseases ; 0.356 0.966
Nonalcoholic Steatohepatitis Digestive System Diseases ; 0.356 0.966
Lymphoma, Diffuse Neoplasms ; Hemic and Lymphatic Diseases ; Immune System Diseases ; 0.356 0.966
Pneumonitis Respiratory Tract Diseases ; 0.356 0.966
Bone marrow failure syndrome 1 Hemic and Lymphatic Diseases ; 0.356 0.966
Bone marrow failure syndrome 2 Hemic and Lymphatic Diseases ; 0.356 0.966
Familial Ménière disease N/A 0.356 0.966
NO RESULT FOUND
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