All terms in UNIPROT
| Label | Id | Description |
|---|---|---|
| Rho-related GTP-binding protein RhoE | Q6SA80 | [Function: Binds GTP but lacks intrinsic GTPase activity and is resistant to Rho-specific GTPase-activating proteins.] |
| Hepatocyte nuclear factor 4-alpha | P49698 | [Function: Transcriptional regulator which controls the expression of hepatic genes during the transition of endodermal cells to hepatic progenitor cells, facilitatating the recruitment of RNA pol II to the promoters of target genes (By similarity). Activates the transcription of CYP2C38 (PubMed:30555544). Represses the CLOCK-ARNTL/BMAL1 transcriptional activity and is essential for circadian rhythm maintenance and period regulation in the liver and colon cells (PubMed:30530698).] |
| Serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B | B2RXR6 | [Function: Putative regulatory subunit of protein phosphatase 6 (PP6) that may be involved in the recognition of phosphoprotein substrates.] |
| Volume-regulated anion channel subunit LRRC8E | Q6NSJ5 | [Function: Non-essential component of the volume-regulated anion channel (VRAC, also named VSOAC channel), an anion channel required to maintain a constant cell volume in response to extracellular or intracellular osmotic changes (PubMed:24790029, PubMed:26824658, PubMed:28193731). The VRAC channel conducts iodide better than chloride and can also conduct organic osmolytes like taurine (PubMed:24790029, PubMed:26824658). Mediates efflux of amino acids, such as aspartate, in response to osmotic stress (PubMed:28193731). Channel activity requires LRRC8A plus at least one other family member (LRRC8B, LRRC8C, LRRC8D or LRRC8E); channel characteristics depend on the precise subunit composition (PubMed:24790029, PubMed:26824658, PubMed:28193731).] |
| Nuclear cap-binding protein subunit 1 | Q3UYV9 | [Function: Component of the cap-binding complex (CBC), which binds cotranscriptionally to the 5'-cap of pre-mRNAs and is involved in various processes such as pre-mRNA splicing, translation regulation, nonsense-mediated mRNA decay, RNA-mediated gene silencing (RNAi) by microRNAs (miRNAs) and mRNA export. The CBC complex is involved in mRNA export from the nucleus via its interaction with ALYREF/THOC4/ALY, leading to the recruitment of the mRNA export machinery to the 5'-end of mRNA and to mRNA export in a 5' to 3' direction through the nuclear pore. The CBC complex is also involved in mediating U snRNA and intronless mRNAs export from the nucleus. The CBC complex is essential for a pioneer round of mRNA translation, before steady state translation when the CBC complex is replaced by cytoplasmic cap-binding protein eIF4E. The pioneer round of mRNA translation mediated by the CBC complex plays a central role in nonsense-mediated mRNA decay (NMD), NMD only taking place in mRNAs bound to the CBC complex, but not on eIF4E-bound mRNAs. The CBC complex enhances NMD in mRNAs containing at least one exon-junction complex (EJC) via its interaction with UPF1, promoting the interaction between UPF1 and UPF2. The CBC complex is also involved in 'failsafe' NMD, which is independent of the EJC complex, while it does not participate in Staufen-mediated mRNA decay (SMD). During cell proliferation, the CBC complex is also involved in microRNAs (miRNAs) biogenesis via its interaction with SRRT/ARS2 and is required for miRNA-mediated RNA interference. The CBC complex also acts as a negative regulator of PARN, thereby acting as an inhibitor of mRNA deadenylation. In the CBC complex, NCBP1/CBP80 does not bind directly capped RNAs (m7GpppG-capped RNA) but is required to stabilize the movement of the N-terminal loop of NCBP2/CBP20 and lock the CBC into a high affinity cap-binding state with the cap structure. Associates with NCBP3 to form an alternative cap-binding complex (CBC) which plays a key role in mRNA export and is particularly important in cellular stress situations such as virus infections. The conventional CBC with NCBP2 binds both small nuclear RNA (snRNA) and messenger (mRNA) and is involved in their export from the nucleus whereas the alternative CBC with NCBP3 does not bind snRNA and associates only with mRNA thereby playing a role only in mRNA export. NCBP1/CBP80 is required for cell growth and viability (By similarity).] |
| Myogenesis-regulating glycosidase | Q6NSJ0 | [Function: Putative glycosidase. Promotes myogenesis by activating AKT signaling through the maturation and secretion of IGF2.] |
| Pleckstrin homology-like domain family B member 3 | Q6NSJ2 | |
| Dynein assembly factor 3, axonemal | Q3UYV8 | [Function: Required for the assembly of axonemal inner and outer dynein arms. Involved in preassembly of dyneins into complexes before their transport into cilia (By similarity).] |
| GDH/6PGL endoplasmic bifunctional protein | Q8CFX1 | [Function: Oxidizes glucose-6-phosphate and glucose, as well as other hexose-6-phosphates.] |
| GTP-binding protein REM 2 | Q8IYK8 | [Function: Binds GTP saturably and exhibits a low intrinsic rate of GTP hydrolysis.] |
| Vacuolar protein sorting-associated protein 33B | P59016 | [Function: May play a role in vesicle-mediated protein trafficking to lysosomal compartments and in membrane docking/fusion reactions of late endosomes/lysosomes. Mediates phagolysosomal fusion in macrophages. Proposed to be involved in endosomal maturation implicating in part VIPAS39 (By similarity). In epithelial cells, the VPS33B:VIPAS39 complex may play a role in the apical RAB11A-dependentrecycling pathway and in the maintenance of the apical-basolateral polarity (PubMed:20190753). Seems to be involved in the sorting of specific cargos from the trans-Golgi network to alpha-granule-destined multivesicular bodies (MVBs) promoting MVBs maturation in megakaryocytes (PubMed:25947942).] |
| Olfactory receptor 13H1 | Q8NG92 | [Function: Odorant receptor.] |
| Bcl-2-like protein 13 | P59017 | [Function: May promote the activation of caspase-3 and apoptosis.] |
| Olfactory receptor 7G3 | Q8NG95 | [Function: Odorant receptor.] |
| Olfactory receptor 11H1 | Q8NG94 | [Function: Odorant receptor.] |
| Procollagen galactosyltransferase 2 | Q8IYK4 | [Function: Beta-galactosyltransferase that transfers beta-galactose to hydroxylysine residues of collagen.] |
| Syntaxin-binding protein 6 | Q8NFX7 | [Function: Forms non-fusogenic complexes with SNAP25 and STX1A and may thereby modulate the formation of functional SNARE complexes and exocytosis.] |
| Olfactory receptor 2Z1 | Q8NG97 | [Function: Odorant receptor.] |
| N-acylneuraminate cytidylyltransferase | Q8NFW8 | [Function: Catalyzes the activation of N-acetylneuraminic acid (NeuNAc) to cytidine 5'-monophosphate N-acetylneuraminic acid (CMP-NeuNAc), a substrate required for the addition of sialic acid. Has some activity toward NeuNAc, N-glycolylneuraminic acid (Neu5Gc) or 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid (KDN).] |
| UPF0688 protein C1orf174 | Q8IYL3 |