PMID: 16097053

Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.

World journal of gastroenterology
H Machida, K Tsukamoto, CY Wen, S Shikuwa, H Isomoto, Y Mizuta, F Takeshima, K Murase, N Matsumoto, I Murata, S Kohno, CY Wen
2005-08-21

5 variants were identified in this publication


Variant ID Gene cDNA Protein Consequence Exon Intron
3-197748392-TG-AC LMLN c.1441_1442delTGinsAC p.Cys481Thr Missense 13/16 -
3-197707219-G-C LMLN c.572G>C p.Gly191Ala Missense 6/16 -
16-50745591-G-C NOD2 c.1769G>C p.Gly590Ala Missense 4/12 -
2-234676965-G-C UGT1A7 c.1175G>C p.Gly392Ala Missense 4/5 -
2-234676516-AC-TG UGT1A3 c.1021_1022delACinsTG p.Thr341Cys Missense 3/5 -