Search Results for: ATXN1

292 interactions involving ATXN1 - ataxin 1 found:

Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
SETD6 SET domain containing 6, protein lysine methyltransferase
  • PKMTs methylate histone lysines
SF1 splicing factor 1
  • mRNA Splicing - Major Pathway
  • Artenimol
SGMS1 sphingomyelin synthase 1
  • Sphingolipid de novo biosynthesis
SLC4A2 solute carrier family 4 member 2
  • Bicarbonate transporters
SOX3 SRY-box transcription factor 3
  • Deactivation of the beta-catenin transactivating complex
  • Septo-optic dysplasia
  • Pituitary Dwarfism (PD); Isolated growth hormone deficiency (IGHD); Short Stature and Pituitary Defects (SSPD); Insulin-like growth factor 1 deficiency (IGFD)
  • 46,XX disorders of sex development (Disorders of gonadal development), including: Ovotesticular DSD; Testicular DSD; Ovarian dysgenesis
  • Syndromic X-linked mental retardation, including: Turner type (MRXST); Siderius type (MRXSSD) ; Cabezas type (MRXC); Raymond type (MRXSR); Type10 (MRXS10); Type14 (MRXS14); Mental retardation with isolated growth hormone deficiency (MRGH)
SUPT20H SPT20 homolog, SAGA complex component
  • HATs acetylate histones
TCAP titin-cap
  • Striated Muscle Contraction
  • Limb-girdle muscular dystrophy (LGMD)
TDP2 tyrosyl-DNA phosphodiesterase 2
  • Nonhomologous End-Joining (NHEJ)
TRIM38 tripartite motif containing 38
  • Interferon gamma signaling
UHRF2 ubiquitin like with PHD and ring finger domains 2
  • SUMOylation of transcription cofactors
WNK1 WNK lysine deficient protein kinase 1
  • Stimuli-sensing channels
  • Hyperkalemic distal renal tubular acidosis (RTA type 4), including the following two diseases: Pseudohypoaldosteronism type I (PHA1); Pseudohypoaldosteronism type II (Gordon's syndrome)
WNK2 WNK lysine deficient protein kinase 2
  • Stimuli-sensing channels
ZSWIM8 zinc finger SWIM-type containing 8
  • Regulation of expression of SLITs and ROBOs
- uncharacterized LOC401442
AHDC1 AT-hook DNA binding motif containing 1
ANKHD1 ankyrin repeat and KH domain containing 1
ARID5A AT-rich interaction domain 5A
ATXN1L ataxin 1 like
ATXN2 ataxin 2
  • Spinocerebellar ataxia (SCA); Machado-Joseph disease (SCA3)
ATXN2L ataxin 2 like

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