ATXN1 - Wiki-MPM

Novel	Interactant Symbol	Name	Associated Pathways Hide	Associated Diseases Hide
Novel	TBC1D5	TBC1 domain family member 5
Novel	TBX15	T-box transcription factor 15		Cousin syndrome
Novel	TCAP	titin-cap	Striated Muscle Contraction	Limb-girdle muscular dystrophy (LGMD)
Novel	TCEANC	transcription elongation factor A N-terminal and central domain containing
Novel	TCTA	T cell leukemia translocation altered
Novel	TDP2	tyrosyl-DNA phosphodiesterase 2	Nonhomologous End-Joining (NHEJ)
Novel	TENT5A	terminal nucleotidyltransferase 5A
Novel	TENT5B	terminal nucleotidyltransferase 5B
Novel	TMX2	thioredoxin related transmembrane protein 2
Novel	TOLLIP	toll interacting protein	Neutrophil degranulation Interleukin-1 signaling
Novel	TOMM20	translocase of outer mitochondrial membrane 20	Mitochondrial protein import PINK1-PRKN Mediated Mitophagy Ub-specific processing proteases
Novel	TOX4	TOX high mobility group box family member 4
Novel	TP53I11	tumor protein p53 inducible protein 11
Novel	TPRX1	tetrapeptide repeat homeobox 1	Zygotic genome activation (ZGA) Zygotic genome activation (ZGA)
Novel	TRAF2	TNF receptor associated factor 2	Caspase activation via Death Receptors in the presence of ligand Regulation by c-FLIP RIPK1-mediated regulated necrosis CASP8 activity is inhibited TNFR1-induced proapoptotic signaling Regulation of TNFR1 signaling TNFR1-induced NF-kappa-B signaling pathway TNFR2 non-canonical NF-kB pathway Regulation of necroptotic cell death TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway Ub-specific processing proteases Dimerization of procaspase-8 TNF signaling TRAF6 mediated IRF7 activation TRAF6 mediated NF-kB activation TRAF6 mediated NF-kB activation Defective RIPK1-mediated regulated necrosis Regulation of NF-kappa B signaling
Novel	TRIM32	tripartite motif containing 32	Regulation of innate immune responses to cytosolic DNA Antigen processing: Ubiquitination & Proteasome degradation	Bardet-Biedl syndrome (BBS)
Novel	TRIM38	tripartite motif containing 38	Interferon gamma signaling
Novel	TRIP6	thyroid hormone receptor interactor 6
Novel	TSC1	TSC complex subunit 1	Macroautophagy Inhibition of TSC complex formation by PKB Energy dependent regulation of mTOR by LKB1-AMPK TP53 Regulates Metabolic Genes TBC/RABGAPs	Lymphangioleiomyomatosis (LAM) Tuberous sclerosis complex (TSC); Bourneville-Pringle disease
Novel	TTC19	tetratricopeptide repeat domain 19	Complex III assembly	Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome

Search Results for: ATXN1