Details of Epigenetic Molecule(EM)

General Information of EM (ID: EM05595)
  Official Symbol
SLC35G1
  Official Full Name
solute carrier family 35 member G1
  Synonym
C10orf60;FLJ33990;TMEM20
  Molecule Type
Protein coding
  Position On Chromosome
chr10(Start:93893973 - End:93956062)
  Strand
+
  Uniprot Entry
Q2M3R5 
  ENSG ID
ENSG00000176273 
  Dnmivd Disease
UCEC 
    Disease Relevance (Click to Show/Hide)
         1C62: Human immunodeficiency virus disease without mention of tuberculosis or malaria Acquired immune deficiency syndrome [Human immunodeficiency virus disease without mention of tuberculosis or malaria]
            Detailed Information Disease Link click to show the detail information of this Disease
         DD70: Crohn disease Crohn's disease [Crohn disease]
            Detailed Information Disease Link click to show the detail information of this Disease
         LD2B: Syndromes with premature ageing appearance as a major feature Werner Syndrome [Syndromes with premature ageing appearance as a major feature]
            Detailed Information Disease Link click to show the detail information of this Disease
         XH8P29: Medulloblastoma Medulloblastoma [Medulloblastoma]
            Detailed Information Disease Link click to show the detail information of this Disease
Protein(s) with this epigenetic modification
  Protein Name: Rv2966c
     Detailed Information Pro Info click to show the detail information of this protein [1]
     Description
Rv2966c could hypermethylate the non-CpG dinucleotides at the host SLC35G1 (geneBody) genetic loci during Mycobacterium tuberculosis H37Rv infection.

References
1 Genome-wide non-CpG methylation of the host genome during M. tuberculosis infection. Sci Rep. 2016 Apr 26;6:25006. doi: 10.1038/srep25006.

If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Tang and Dr. Zhang.