Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.120 GeneticVariation BEFREE Epigenetics, presume to be the mechanistic link between environmental and genetic risk factors in disease development, provides support for specific microRNAs associated with MG. Genetic studies have mainly pointed at specific HLA alleles implicated in MG susceptibility, however recently both TNFAIP3-interacting protein 1 (TNIP1) and tyrosine phosphatase non-receptor 22 (PTPN22) were indicated to be associated with MG in a GWAS study. 24361103

2014
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.120 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271

2012
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.120 GeneticVariation BEFREE Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271

2012