Search Results for: ARL13B

Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
TMUB2 transmembrane and ubiquitin like domain containing 2
TNFRSF10C TNF receptor superfamily member 10c
  • TP53 Regulates Transcription of Death Receptors and Ligands
TNMD tenomodulin
TRARG1 trafficking regulator of GLUT4 (SLC2A4) 1
TSPO2 translocator protein 2
UBE2I ubiquitin conjugating enzyme E2 I
  • Meiotic synapsis
  • Vitamin D (calciferol) metabolism
  • SUMO is transferred from E1 to E2 (UBE2I, UBC9)
  • SUMO is transferred from E1 to E2 (UBE2I, UBC9)
  • SUMOylation of DNA damage response and repair proteins
  • SUMO E3 ligases SUMOylate target proteins
  • SUMOylation of transcription factors
  • SUMOylation of transcription factors
  • SUMOylation of ubiquitinylation proteins
  • SUMOylation of transcription cofactors
  • SUMOylation of transcription cofactors
  • SUMOylation of SUMOylation proteins
  • SUMOylation of intracellular receptors
  • SUMOylation of intracellular receptors
  • SUMOylation of chromatin organization proteins
  • SUMOylation of chromatin organization proteins
  • SUMOylation of RNA binding proteins
  • SUMOylation of DNA replication proteins
  • SUMOylation of DNA replication proteins
  • SUMOylation of DNA methylation proteins
  • SUMOylation of DNA methylation proteins
  • SUMOylation of immune response proteins
  • Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
  • Processing of DNA double-strand break ends
  • Formation of Incision Complex in GG-NER
  • Negative regulation of activity of TFAP2 (AP-2) family transcription factors
  • Negative regulation of activity of TFAP2 (AP-2) family transcription factors
  • Postmitotic nuclear pore complex (NPC) reformation
  • Maturation of nucleoprotein
  • Maturation of nucleoprotein
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
  • Botulinum Toxin Type B
VAMP3 vesicle associated membrane protein 3
  • ER-Phagosome pathway
  • Retrograde transport at the Trans-Golgi-Network
  • Cargo recognition for clathrin-mediated endocytosis
  • Clathrin-mediated endocytosis
VAMP4 vesicle associated membrane protein 4
  • Retrograde transport at the Trans-Golgi-Network
  • Cargo recognition for clathrin-mediated endocytosis
  • Clathrin-mediated endocytosis
VSTM1 V-set and transmembrane domain containing 1
WFDC2 WAP four-disulfide core domain 2
YIPF6 Yip1 domain family member 6
  • Golgi Associated Vesicle Biogenesis
ZDHHC15 zinc finger DHHC-type 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)

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