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MMEL1 and celiac disease are reported together in 1 article.
Gene
MMEL1
- HGNC
- HGNC:14668
1articles
1mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Celiac disease
74articles
74mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients.
PMID 26843707 | PMCID PMC4710944 | DOI 10.1155/2015/351673 · Disease markers · 2015 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MMEL1 | “Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients.” | 0.98 | hgnc_dict_v1 |
| phenotype | celiac disease | “Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | IRAK1 | “Therefore, we genotyped Saudi CD patients and healthy controls for three polymorphisms, that is, Phe196Ser in IRAK1, Trp262Arg in SH2B3, and Met518Thr in MMEL1 genes.” | 0.98 | hgnc_dict_v1 |
| gene | SH2B3 | “Therefore, we genotyped Saudi CD patients and healthy controls for three polymorphisms, that is, Phe196Ser in IRAK1, Trp262Arg in SH2B3, and Met518Thr in MMEL1 genes.” | 0.98 | hgnc_dict_v1 |