| Name |
|---|
HYPERGLYCINURIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERGLYCINURIA from the curated CTD Gene-Disease Associations dataset. |
hyperglycinuria Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperglycinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperglycinuria Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperglycinuria phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperglycinuria Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hyperglycinuria phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Hyperglycinuria Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperglycinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperglycinuria (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperglycinuria (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG) Gene Setproteins participating in the Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG) pathway from the Reactome Pathways 2024 dataset. |
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_5619101 Gene Setproteins participating in the Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_5619101 pathway from the Reactome Pathways 2024 dataset. |
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_5660686 Gene Setproteins participating in the Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_5660686 pathway from the Reactome Pathways 2024 dataset. |