Details of Epigenetic Molecule(EM)

General Information of EM (ID: EM12400)
  Official Symbol
SLC6A19
  Official Full Name
Solute Carrier Family 6 Member 19
  Synonym
Solute Carrier Family 6 Member 19;Solute Carrier Family 6 (Neutral Amino Acid Transporter), Member 19;Sodium-Dependent Neutral Amino Acid Transporter B(0)AT1;System B(0) Neutral Amino Acid Transporter AT1;B0AT1;Sodium-Dependent Amino Acid Transporter System B0;System B0 Neutral Amino Acid Transporter;Hartnup Disease;HND
  Molecule Type
Protein coding
  Position On Chromosome
chr5(Start:1201595 - End:1225111)
  Strand
+
  Uniprot Entry
Q695T7 
  ENSG ID
ENSG00000174358 
    Disease Relevance (Click to Show/Hide)
         2C30: Melanoma of skin Cutaneous Melanoma [Melanoma of skin]
            Detailed Information Disease Link click to show the detail information of this Disease
         8A00: Parkinsonism Parkinson's disease (PD) [Parkinsonism]
            Detailed Information Disease Link click to show the detail information of this Disease
         8A01: Choreiform disorders Huntington's disease (HD) [Choreiform disorders]
            Detailed Information Disease Link click to show the detail information of this Disease
         8A20: Alzheimer disease Alzheimer's disease [Alzheimer disease]
            Detailed Information Disease Link click to show the detail information of this Disease
         CB03: Idiopathic interstitial pneumonitis Idiopathic pulmonary fibrosis (IPF) [Idiopathic interstitial pneumonitis]
            Detailed Information Disease Link click to show the detail information of this Disease
         LD2C: Overgrowth syndromes Sotos syndrome(SS) [Overgrowth syndromes]
            Detailed Information Disease Link click to show the detail information of this Disease
         LD2FZERO(Not Found)0: Toxic or drug-related embryofetopathies Fetal alcohol spectrum disorder (FASD) [Toxic or drug-related embryofetopathies]
            Detailed Information Disease Link click to show the detail information of this Disease
         SE30: Developmental delay disorder CHARGE and Kabuki syndromes [Developmental delay disorder]
            Detailed Information Disease Link click to show the detail information of this Disease
         XH5QN3: Nephroblastoma Wilms tumor [Nephroblastoma]
            Detailed Information Disease Link click to show the detail information of this Disease
Metabolite(s) with this epigenetic modification
  Metabolite Name: Arachidonic acid
     Detailed Information Meta Info click to show the detail information of this Metabolite [1], [2]
     Description
Arachidonic acid could induce SLC6A19 gene hypermethylation in THP-1 cells.

References
1 Gut Microbiota as Important Mediator Between Diet and DNA Methylation and Histone Modifications in the Host. Nutrients. 2020 Feb 25;12(3):597. doi: 10.3390/nu12030597.
2 Arachidonic and oleic acid exert distinct effects on the DNA methylome. Epigenetics. 2016 May 3;11(5):321-34. doi: 10.1080/15592294.2016.1161873. Epub 2016 Apr 18.

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