CREB3L1 - New-wiki

Interactant Symbol	Name	Associated Pathways Hide	Binding Drugs Hide	Associated Diseases Hide
TNF	tumor necrosis factor	Transcriptional regulation of white adipocyte differentiation TNFR1-induced proapoptotic signaling Regulation of TNFR1 signaling TNFR1-induced NF-kappa-B signaling pathway TNFR1-mediated ceramide production TNFR2 non-canonical NF-kB pathway Interleukin-10 signaling Interleukin-4 and Interleukin-13 signaling TNF signaling Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells)	Etanercept Adalimumab Infliximab Chloroquine Epinephrine Pseudoephedrine Clenbuterol Pranlukast Amrinone Trichostatin A Afelimomab YSIL6 SD118 PN0621 OMS-103HP Talmapimod VX-702 Atiprimod CRx-139 CYT007-TNFQb Andrographolide Ethyl pyruvate AME-527 PR-104 Plinabulin Dexanabinol Onercept Golimumab Certolizumab pegol Pomalidomide Polaprezinc Foreskin fibroblast (neonatal) Foreskin keratinocyte (neonatal) Bryostatin 1 Binimetinib Dilmapimod Glycyrrhizic acid	Graft-versus-host disease Systemic lupus erythematosus Allograft rejection Asthma
TNFRSF10C	TNF receptor superfamily member 10c	TP53 Regulates Transcription of Death Receptors and Ligands
TNMD	tenomodulin
TRAM1L1	translocation associated membrane protein 1 like 1
TSPAN2	tetraspanin 2
TSPO	translocator protein	Pregnenolone biosynthesis	Chlormezanone Zopiclone
TSPO2	translocator protein 2
UBIAD1	UbiA prenyltransferase domain containing 1	Metabolism of vitamin K		Schnyder corneal dystrophy (SCD); Schnyder crystalline corneal dystrophy (SCCD); Crystalline stromal dystrophy; Schnyder crystalline dystrophy sine crystals
UNC93B1	unc-93B1 regulator of TLR signaling	Trafficking and processing of endosomal TLR UNC93B1 deficiency - HSE
VAMP1	vesicle associated membrane protein 1	Toxicity of botulinum toxin type D (botD) Toxicity of botulinum toxin type F (botF) Toxicity of botulinum toxin type G (botG)	Botulinum toxin type B
VAMP2	vesicle associated membrane protein 2	Translocation of SLC2A4 (GLUT4) to the plasma membrane Serotonin Neurotransmitter Release Cycle Norepinephrine Neurotransmitter Release Cycle trans-Golgi Network Vesicle Budding Glutamate Neurotransmitter Release Cycle Dopamine Neurotransmitter Release Cycle Acetylcholine Neurotransmitter Release Cycle Insulin processing Regulation of insulin secretion Lysosome Vesicle Biogenesis Golgi Associated Vesicle Biogenesis Other interleukin signaling Toxicity of botulinum toxin type D (botD) Toxicity of botulinum toxin type B (botB) Toxicity of botulinum toxin type F (botF) Toxicity of tetanus toxin (tetX) Toxicity of botulinum toxin type G (botG) Cargo recognition for clathrin-mediated endocytosis Clathrin-mediated endocytosis GABA synthesis, release, reuptake and degradation Insertion of tail-anchored proteins into the endoplasmic reticulum membrane Insertion of tail-anchored proteins into the endoplasmic reticulum membrane Sensory processing of sound by inner hair cells of the cochlea	Botulinum toxin type B
VEZT	vezatin, adherens junctions transmembrane protein
VKORC1	vitamin K epoxide reductase complex subunit 1	Metabolism of vitamin K	Menadione Dicoumarol Phenindione Warfarin Phenprocoumon Acenocoumarol	Combined deficiency of vitamin K-dependent clotting factors (VKCFD)
WFDC2	WAP four-disulfide core domain 2	Formation of the nephric duct
YIPF6	Yip1 domain family member 6	Golgi Associated Vesicle Biogenesis
ZDHHC15	zDHHC palmitoyltransferase 15			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)
ZDHHC22	zDHHC palmitoyltransferase 22
ZFPL1	zinc finger protein like 1

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