Search Results for: ATXN1

292 interactions involving ATXN1 - ataxin 1 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
MBP myelin basic protein
  • EGR2 and SOX10-mediated initiation of Schwann cell myelination
MSMO1 methylsterol monooxygenase 1
  • Cholesterol biosynthesis
  • NADH
MSX2 msh homeobox 2
  • Regulation of RUNX2 expression and activity
  • Enlarged parietal foramina/cranium bifidum
  • 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
MTERF4 mitochondrial transcription termination factor 4
  • rRNA modification in the mitochondrion
NARS1 asparaginyl-tRNA synthetase 1
  • Cytosolic tRNA aminoacylation
  • Asparagine
NLK nemo like kinase
  • Ca2+ pathway
NPHP3 nephrocystin 3
  • Trafficking of myristoylated proteins to the cilium
  • Senior-Loken syndrome
  • Renal-hepatic-pancreatic dysplasia
  • Nephronophthisis-medullary cystic kidney disease, including; Nephronophthisis (NPH) ; Nephronophthisis-like nephropathy 1; Medullary cystic kidney disease 1; Medullary cystic kidney disease 2 (MSKD2)
  • Meckel syndrome (MKS); Meckel-Gruber syndrome
OAZ1 ornithine decarboxylase antizyme 1
  • Regulation of ornithine decarboxylase (ODC)
  • Ornithine
OPCML opioid binding protein/cell adhesion molecule like
  • Post-translational modification: synthesis of GPI-anchored proteins
PANX2 pannexin 2
  • Electric Transmission Across Gap Junctions
PPAT phosphoribosyl pyrophosphate amidotransferase
  • Purine ribonucleoside monophosphate biosynthesis
  • L-Glutamine
  • Mercaptopurine
  • Dasatinib
PQBP1 polyglutamine binding protein 1
  • mRNA Splicing - Major Pathway
  • 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)
  • Non-syndromic X-linked mental retardation
PRDM1 PR/SET domain 1
  • Regulation of TP53 Expression
PSPH phosphoserine phosphatase
  • Serine biosynthesis
  • Zinc
  • 3-Phosphono-D-alanine
  • Zinc acetate
  • Zinc chloride
  • Zinc sulfate, unspecified form
PUM1 pumilio RNA binding family member 1
  • Golgi Associated Vesicle Biogenesis
QKI QKI, KH domain containing RNA binding
  • Signaling by BRAF and RAF fusions
RBFOX1 RNA binding fox-1 homolog 1
  • MECP2 regulates transcription factors
RBFOX2 RNA binding fox-1 homolog 2
  • FGFR2 alternative splicing
REL REL proto-oncogene, NF-kB subunit
  • Activation of NF-kappaB in B cells
  • Hodgkin lymphoma
SETD2 SET domain containing 2, histone lysine methyltransferase
  • PKMTs methylate histone lysines

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