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ERBB4
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erb-b2 receptor tyrosine kinase 4 |
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- Afatinib
- Fostamatinib
- Brigatinib
- Zanubrutinib
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ERG28
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ergosterol biosynthesis 28 homolog |
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EYA4
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EYA transcriptional coactivator and phosphatase 4 |
- Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
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EZR
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ezrin |
- Netrin-1 signaling
- Recycling pathway of L1
- Recycling pathway of L1
- Sensory processing of sound by inner hair cells of the cochlea
- Sensory processing of sound by outer hair cells of the cochlea
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FAM241B
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family with sequence similarity 241 member B |
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FER
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FER tyrosine kinase |
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FES
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FES proto-oncogene, tyrosine kinase |
- Signaling by SCF-KIT
- Sema3A PAK dependent Axon repulsion
- SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
- CRMPs in Sema3A signaling
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FGFR1
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fibroblast growth factor receptor 1 |
- Signaling by activated point mutants of FGFR1
- Signaling by FGFR1 in disease
- Signaling by plasma membrane FGFR1 fusions
- Epithelial-Mesenchymal Transition (EMT) during gastrulation
- Formation of paraxial mesoderm
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- Palifermin
- Sorafenib
- Heparin
- 3-[4-(1-formylpiperazin-4-yl)-benzylidenyl]-2-indolinone
- XL999
- 3-(3-methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine
- (E)-[4-(3,5-Difluorophenyl)-3H-pyrrolo[2,3-b]pyridin-3-ylidene](3-methoxyphenyl)methanol
- 3-[(3-(2-CARBOXYETHYL)-4-METHYLPYRROL-2-YL)METHYLENE]-2-INDOLINONE
- Regorafenib
- Ponatinib
- Lenvatinib
- Nintedanib
- Tivozanib
- Infigratinib
- Fostamatinib
- Erdafitinib
- Pemigatinib
- Futibatinib
- Selpercatinib
- Pralsetinib
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- Hypogonadotropic hypogonadism; Kallmann syndrome (KAL)
- Craniosynostosis, including: Pfeiffer syndrome; Apert syndrome; Crouzon syndrome; Jackson-Weiss syndrome; Beare-Stevenson syndrome; Muenke craniosynostosis; Saethre-Chotzen syndrome; Craniosynostosis Boston type; Antley-Bixler syndrome; Carpenter syndrome; Craniofrontonasal dysplasia; Noonan syndrome; Baller-Gerold syndrome
- Osteoglophonic dysplasia (OD); Osteoglophonic dwarfism (OGD)
- Isolated orofacial clefts, including: Cleft lip with or without cleft palate; Cleft palate
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FGR
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FGR proto-oncogene, Src family tyrosine kinase |
- FCGR activation
- Platelet sensitization by LDL
- Neutrophil degranulation
- FCGR3A-mediated IL10 synthesis
- FCGR3A-mediated phagocytosis
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- Dasatinib
- Fostamatinib
- Zanubrutinib
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FHL3
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four and a half LIM domains 3 |
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FKBP1A
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FKBP prolyl isomerase 1A |
- mTORC1-mediated signalling
- Calcineurin activates NFAT
- Calcineurin activates NFAT
- TGF-beta receptor signaling activates SMADs
- TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)
- TGFBR1 LBD Mutants in Cancer
- Potential therapeutics for SARS
- SARS-CoV-1 activates/modulates innate immune responses
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- Pimecrolimus
- Tacrolimus
- (3R)-4-(p-toluenesulfonyl)-1,4-thiazane-3-carboxylicacid-L-phenylalanine ethyl ester
- {3-[3-(3,4-Dimethoxy-Phenyl)-1-(1-{1-[2-(3,4,5-Trimethoxy-Phenyl)-Butyryl]-Piperidin-2yl}-Vinyloxy)-Propyl]-Phenoxy}-Acetic Acid
- Gpi-1046
- Methyl Methylsulfinylmethyl Sulfide
- FKB-001
- Heptyl glucoside
- L-709,587
- (3r)-4-(P-Toluenesulfonyl)-1,4-Thiazane-3-Carboxylicacid-L-Leucine
- 4-hydroxybutan-2-one
- GPI-1485
- Myristic acid
- (21S)-1AZA-4,4-DIMETHYL-6,19-DIOXA-2,3,7,20-TETRAOXOBICYCLO[19.4.0] PENTACOSANE
- Dorsomorphin
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FLNA
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filamin A |
- Platelet degranulation
- GP1b-IX-V activation signalling
- Cell-extracellular matrix interactions
- RHO GTPases activate PAKs
- OAS antiviral response
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- FG syndrome (FGS); Opitz-Kaveggia syndrome
- Periventricular nodular heterotopia (PVNH)
- Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
- Fronto-Otopalatodigital Osteodysplasia, including: Otopalatodigital syndrome, type I; Otopalatodigital syndrome, type II; Melnick-Needles syndrome; Frontometaphyseal dysplasia
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FLYWCH1
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FLYWCH-type zinc finger 1 |
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GABARAPL1
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GABA type A receptor associated protein like 1 |
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GABARAPL2
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GABA type A receptor associated protein like 2 |
- Macroautophagy
- TBC/RABGAPs
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GRAP2
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GRB2 related adaptor protein 2 |
- Signaling by SCF-KIT
- Generation of second messenger molecules
- DAP12 signaling
- FCERI mediated MAPK activation
- FCERI mediated Ca+2 mobilization
- FCERI mediated Ca+2 mobilization
- Co-stimulation by CD28
- FLT3 Signaling
- Signaling by CSF1 (M-CSF) in myeloid cells
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GRB2
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growth factor receptor bound protein 2 |
- Interleukin-15 signaling
- Interleukin-15 signaling
- Signaling by CSF3 (G-CSF)
- Signaling by CSF3 (G-CSF)
- STAT5 activation downstream of FLT3 ITD mutants
- Signaling by FLT3 ITD and TKD mutants
- Signaling by FLT3 ITD and TKD mutants
- Signaling by ALK fusions and activated point mutants
- Signaling by LTK
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- Pegademase
- 4-[(10s,14s,18s)-18-(2-Amino-2-Oxoethyl)-14-(1-Naphthylmethyl)-8,17,20-Trioxo-7,16,19-Triazaspiro[5.14]Icos-11-En-10-Yl]Benzylphosphonic Acid
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GRB7
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growth factor receptor bound protein 7 |
- GRB7 events in ERBB2 signaling
- Signaling by SCF-KIT
- Downstream signal transduction
- Tie2 Signaling
- RET signaling
- RND1 GTPase cycle
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HCK
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HCK proto-oncogene, Src family tyrosine kinase |
- Nef and signal transduction
- FCGR activation
- Regulation of signaling by CBL
- Regulation of signaling by CBL
- FCGR3A-mediated IL10 synthesis
- FCGR3A-mediated phagocytosis
- Signaling by CSF3 (G-CSF)
- Signaling by CSF3 (G-CSF)
- Signaling by CSF1 (M-CSF) in myeloid cells
- Inactivation of CSF3 (G-CSF) signaling
- Inactivation of CSF3 (G-CSF) signaling
- FLT3 signaling through SRC family kinases
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- 1-Ter-Butyl-3-P-Tolyl-1h-Pyrazolo[3,4-D]Pyrimidin-4-Ylamine
- Phosphonotyrosine
- Quercetin
- Bosutinib
- Fostamatinib
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HDAC6
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histone deacetylase 6 |
- NOTCH1 Intracellular Domain Regulates Transcription
- Constitutive Signaling by NOTCH1 PEST Domain Mutants
- Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
- HSF1 activation
- Notch-HLH transcription pathway
- Cargo trafficking to the periciliary membrane
- Transcriptional regulation by RUNX2
- RUNX2 regulates osteoblast differentiation
- Chaperone Mediated Autophagy
- Late endosomal microautophagy
- Aggrephagy
- Aggrephagy
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- Valproic acid
- Decitabine
- Vorinostat
- Vorinostat
- Belinostat
- Pracinostat
- Romidepsin
- Romidepsin
- Panobinostat
- Phenylbutyric acid
- Entinostat
- Abexinostat
- Givinostat
- Pyroxamide
- Bufexamac
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