Search Results for: MRPS25

Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
Novel CAND2 cullin associated and neddylation dissociated 2 (putative)
Novel COLQ collagen like tail subunit of asymmetric acetylcholinesterase
  • Congenital myasthenic syndrome
Novel FBLN2 fibulin 2
  • Molecules associated with elastic fibres
  • Molecules associated with elastic fibres
Novel HDAC11 histone deacetylase 11
  • NOTCH1 Intracellular Domain Regulates Transcription
  • Constitutive Signaling by NOTCH1 PEST Domain Mutants
  • Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
  • Notch-HLH transcription pathway
  • Belinostat
  • Panobinostat
Novel MKRN2 makorin ring finger protein 2
Novel NUAK1 NUAK family kinase 1
  • Regulation of TP53 Activity through Phosphorylation
  • Fostamatinib
Novel XPC XPC complex subunit, DNA damage recognition and repair factor
  • SUMOylation of DNA damage response and repair proteins
  • DNA Damage Recognition in GG-NER
  • Formation of Incision Complex in GG-NER
  • Disorders of nucleotide excision repair, including: Xeroderma pigmentosum (XP); Cockayne syndrome (CS); UV-sensitive syndrome (UVS); Trichothiodystrophy (TTD); Cerebro-oculo-facio-skeletal syndrome (COFS); XFE progeroid syndrome
ERCC6 ERCC excision repair 6, chromatin remodeling factor
  • ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
  • B-WICH complex positively regulates rRNA expression
  • Formation of TC-NER Pre-Incision Complex
  • Transcription-Coupled Nucleotide Excision Repair (TC-NER)
  • Dual incision in TC-NER
  • Gap-filling DNA repair synthesis and ligation in TC-NER
  • RNA Polymerase I Transcription Initiation
  • Disorders of nucleotide excision repair, including: Xeroderma pigmentosum (XP); Cockayne syndrome (CS); UV-sensitive syndrome (UVS); Trichothiodystrophy (TTD); Cerebro-oculo-facio-skeletal syndrome (COFS); XFE progeroid syndrome
  • Cockayne syndrome
  • Macular degeneration, including: Age-related macular degeneration (ARMD); Patterned dystrophy of retinal pigment epithelium (PDREP); Retinal macular dystrophy 2 (MCDR2); X-linked atrophic macular degeneration (MDXLA)

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