ATG16L1, autophagy related 16 like 1, 55054

N. diseases: 120; N. variants: 31
Disease: Inflammatory Bowel Disease 10 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT The Thr300Ala variant in ATG16L1 is associated with improved survival in human colorectal cancer and enhanced production of type I interferon. 25645662 2016
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT The T300A Crohn's disease risk polymorphism impairs function of the WD40 domain of ATG16L1. 27273576 2016
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience. 24656308 2014
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT A Crohn's disease variant in Atg16l1 enhances its degradation by caspase 3. 24553140 2014
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children. 18985712 2009
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children. 19659808 2009
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands. 18047540 2008
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients. 18499543 2008
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5. 17484864 2007
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. 17200669 2007
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1970207
Disease:
Inflammatory Bowel Disease 10 		0.700 GeneticVariation UNIPROT Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756 2007