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DYM and dyslipidemia are reported together in 1 article.
Gene
DYM
- HGNC
- HGNC:21317
7articles
7mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
skeletal dysplasia 5intellectual disability 3celiac disease 1coronary artery disease 1developmental delay 1dyslipidemia 1mucopolysaccharidosis 1
Reported variants (articles · ClinVar status)
Phenotype
Dyslipidemia
338articles
338mentions
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 60Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.
PMID 37668737 | DOI 10.1007/s00335-023-10017-0 · Mammalian genome : official journal of the International Mammalian Genome Society · 2023 · 13 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | DYM | “We identified an association between dyslipidemia and variants identified in genes such as JCAD, GLIS3, CD38, FN1, CELSR2, MTNR1B, GIPR, DYM, APOB, APOE, ADCY5.” | 0.98 | hgnc_dict_v1 |
| phenotype | dyslipidemia | “Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | JCAD | “We identified an association between dyslipidemia and variants identified in genes such as JCAD, GLIS3, CD38, FN1, CELSR2, MTNR1B, GIPR, DYM, APOB, APOE, ADCY5.” | 0.98 | hgnc_dict_v1 |
| gene | GLIS3 | “We identified an association between dyslipidemia and variants identified in genes such as JCAD, GLIS3, CD38, FN1, CELSR2, MTNR1B, GIPR, DYM, APOB, APOE, ADCY5.” | 0.98 | hgnc_dict_v1 |