Name

homozygous Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term homozygous in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Homozygous 11p15-p14 Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homozygous 11p15-p14 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Brn3a_KO_GDS1651_248_mouse_Embryonic (day 13.5) trigeminal ganglia - homozygous Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Brn3a_KO_GDS1651_248_mouse_Embryonic (day 13.5) trigeminal ganglia - homozygous gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

ESRRG_Deficiency_GDS2811_638_mouse_Fetal heart - Homozygous null mutant Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the ESRRG_Deficiency_GDS2811_638_mouse_Fetal heart - Homozygous null mutant gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

ADNP_Deficiency - NULL MUTATION_GDS2540_692_mouse_E9 embryos - Homozygous mutant Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the ADNP_Deficiency - NULL MUTATION_GDS2540_692_mouse_E9 embryos - Homozygous mutant gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

Homozygous Alpha Thalassemia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Homozygous Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Homozygous Factor V Leiden Mutation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Homozygous Factor V Leiden Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Classical Galactosemia, Homozygous Duarte-Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Classical Galactosemia, Homozygous Duarte-Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Homozygous Acute Intermittent Porphyria Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Homozygous Acute Intermittent Porphyria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Homozygous Variegate Porphyria Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Homozygous Variegate Porphyria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Homozygous Protein S Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Homozygous Protein S Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Homozygous familial hypercholesterolemia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Homozygous familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.