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RHOXF2 |
Rhox homeobox family member 2 |
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RIBC1 |
RIB43A domain with coiled-coils 1 |
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RIMBP3 |
RIMS binding protein 3 |
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RIPPLY1 |
ripply transcriptional repressor 1 |
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RNF31 |
ring finger protein 31 |
- Regulation of TNFR1 signaling
- TNFR1-induced NFkappaB signaling pathway
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RORB |
RAR related orphan receptor B |
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RPL18A |
ribosomal protein L18a |
- L13a-mediated translational silencing of Ceruloplasmin expression
- Peptide chain elongation
- SRP-dependent cotranslational protein targeting to membrane
- SRP-dependent cotranslational protein targeting to membrane
- Viral mRNA Translation
- Selenocysteine synthesis
- Major pathway of rRNA processing in the nucleolus and cytosol
- Formation of a pool of free 40S subunits
- GTP hydrolysis and joining of the 60S ribosomal subunit
- Eukaryotic Translation Termination
- Regulation of expression of SLITs and ROBOs
- Response of EIF2AK4 (GCN2) to amino acid deficiency
- Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
- Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
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RUNX1 |
RUNX family transcription factor 1 |
- Pre-NOTCH Transcription and Translation
- Organic cation transport
- RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs)
- RUNX1 regulates estrogen receptor mediated transcription
- Regulation of RUNX1 Expression and Activity
- Regulation of RUNX1 Expression and Activity
- RUNX1 regulates expression of components of tight junctions
- RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
- RUNX1 regulates transcription of genes involved in differentiation of HSCs
- RUNX1 regulates transcription of genes involved in differentiation of HSCs
- RUNX1 regulates transcription of genes involved in differentiation of keratinocytes
- RUNX1 regulates transcription of genes involved in differentiation of keratinocytes
- RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
- RUNX1 regulates transcription of genes involved in BCR signaling
- RUNX1 regulates transcription of genes involved in differentiation of myeloid cells
- RUNX1 regulates transcription of genes involved in interleukin signaling
- RUNX1 regulates transcription of genes involved in WNT signaling
- RUNX2 regulates genes involved in differentiation of myeloid cells
- RUNX3 regulates p14-ARF
- Estrogen-dependent gene expression
- Transcriptional regulation of granulopoiesis
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- Chronic myeloid leukemia (CML)
- Thrombocytopenia (THC); Familial platelet disorder with associated myeloid malignancy (FPDMM)
- Acute myeloid leukemia (AML)
- Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia)
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RUSC1 |
RUN and SH3 domain containing 1 |
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SAT1 |
spermidine/spermine N1-acetyltransferase 1 |
- Interconversion of polyamines
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- N-ethyl-N-[3-(propylamino)propyl]propane-1,3-diamine
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- Keratosis follicularis spinulosa decalvans
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SCNM1 |
sodium channel modifier 1 |
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SDCBP |
syndecan binding protein |
- Ephrin signaling
- Neurofascin interactions
- RIPK1-mediated regulated necrosis
- Regulation of necroptotic cell death
- Neutrophil degranulation
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SERTAD3 |
SERTA domain containing 3 |
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SET |
SET nuclear proto-oncogene |
- Condensation of Prophase Chromosomes
- HuR (ELAVL1) binds and stabilizes mRNA
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SF3B4 |
splicing factor 3b subunit 4 |
- mRNA Splicing - Major Pathway
- mRNA Splicing - Minor Pathway
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SH2B2 |
SH2B adaptor protein 2 |
- Regulation of KIT signaling
- Factors involved in megakaryocyte development and platelet production
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SH3GL3 |
SH3 domain containing GRB2 like 3, endophilin A3 |
- EGFR downregulation
- Negative regulation of MET activity
- Cargo recognition for clathrin-mediated endocytosis
- Clathrin-mediated endocytosis
- InlB-mediated entry of Listeria monocytogenes into host cell
- NGF-stimulated transcription
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SHFL |
shiftless antiviral inhibitor of ribosomal frameshifting |
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SHISA6 |
shisa family member 6 |
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SIX1 |
SIX homeobox 1 |
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- Contiguous gene deletion syndrome involving EYA1, including: Oto-facio-cervical syndrome (OFC); Branchiootic syndrome 1 (BOS1); Branchio-oto-renal syndrome (BOR)
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