Receptor tyrosine kinase (RTK) family (Homo sapiens)
From WikiPathways
Description
An annotated list of receptor tyrosine kinase (RTK) genes
Quality Tags
Ontology Terms
Pathway Ontology : iron uptake pathway inborn error of metabolism pathway inborn error of metal metabolism pathway altered iron homeostasis pathway iron homeostasis pathway regulatory pathway
Disease : GRACILE syndrome mitochondrial complex III deficiency hemochromatosis type 1 iron metabolism disease hemosiderosis neurodegeneration with brain iron accumulation hemochromatosis type 2B aceruloplasminemia neurodegeneration with brain iron accumulation 3 hemochromatosis type 2A hemochromatosis type 3 hyperferritinemia-cataract syndrome hypochromic microcytic anemia hemochromatosis type 5 pulmonary hemosiderosis atransferrinemia hemochromatosis type 4 immunodeficiency 46 inherited metabolic disorder
Cell Type : native cell enterocyte
Bibliography
- Ségaliny AI, Tellez-Gabriel M, Heymann MF, Heymann D; ''Receptor tyrosine kinases: Characterisation, mechanism of action and therapeutic interests for bone cancers.''; J Bone Oncol, 2015 PubMed Europe PMC Scholia
History
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External references
DataNodes
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Annotated Interactions
No annotated interactions