association dataset threshold value standardized value PMC10663741-mmc4.xlsx-markers_table_FE_ELP_stage-gene_NR5A1 Rummagene Transcription Factor Associations 2026 1.0 null PMC5195898-NIHMS825571-supplement-3.xlsx-Sheet1-H1975_M1_vs_H1975_M1_CIC_reconstitution_Differential_gene_expression_CIC Rummagene Transcription Factor Associations 2026 1.0 null cellular component assembly GO Biological Process Annotations 2015 1.0 null Pulmonary Arterial Hypertension DisGeNET Gene-Disease Associations 1.0 null microcephaly HPO Gene-Disease Associations 1.0 null Adenosine Triphosphate CTD Gene-Chemical Interactions 1.0 null abnormal urinary electrolyte concentration HPO Gene-Disease Associations 1.0 null Clonus DisGeNET Gene-Phenotype Associations 1.0 null Tetralogy Of Fallot DisGeNET Gene-Disease Associations 1.0 null protein complex subunit organization GO Biological Process Annotations 2015 1.0 null respiratory chain complex iv assembly GO Biological Process Annotations 2015 1.0 null PMC9013128-NIHMS1795992-supplement-4.xlsx-501mel_ARID2_KO_Downregulated-Gene__name_ARID2 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the parathyroid gland HPO Gene-Disease Associations 1.0 null abnormality of peripheral nerves HPO Gene-Disease Associations 1.0 null cerebral cortical atrophy HPO Gene-Disease Associations 1.0 null Hemianopsia DisGeNET Gene-Disease Associations 1.0 null Hypothyroidism DisGeNET Gene-Disease Associations 1.0 null PMC6317254__F2 PFOCR Pathway Figure Associations 2024 1.0 null Fatty Liver CTD Gene-Disease Associations 1.0 1.66878 smooth muscle HPA Tissue Protein Expression Profiles -1.0 -1.35386 microdeletion GeneRIF Biological Term Annotations 1.0 null myopathy HPO Gene-Disease Associations 1.0 null abnormality of central motor function HPO Gene-Disease Associations 1.0 null Malignant Neoplasm DisGeNET Gene-Disease Associations 1.0 null Skeletal Muscle Atrophy DisGeNET Gene-Phenotype Associations 1.0 null ichthyosis HPO Gene-Disease Associations 1.0 null headache HPO Gene-Disease Associations 1.0 null Progressive Sensorineural Hearing Impairment DisGeNET Gene-Disease Associations 1.0 null spiral GeneRIF Biological Term Annotations 1.0 null plicamycin_homo sapiens_gpl570_gse25127 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null PMC9882185-media-4.xlsx-Neuron_KD-gene_name_AR Rummagene Transcription Factor Associations 2026 1.0 null PMC6643872__F2 PFOCR Pathway Figure Associations 2024 1.0 null PMC9904760-elife-79363-supp2.xlsx-MDS1-Gene_MECOM Rummagene Transcription Factor Associations 2026 1.0 null Constipation DisGeNET Gene-Phenotype Associations 1.0 null abnormality of blood and blood-forming tissues HPO Gene-Disease Associations 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-NEUN_UNIQUE_DYS_GENES-OLIG2_TLE_vs_TL_log2FoldChange_1_padj_0_1_OLIG2 Rummagene Transcription Factor Associations 2026 1.0 null colorectal cancer GAD Gene-Disease Associations 1.0 null ciprofloxacin_pseudomonas aeruginosa; pseudomonas aeruginosa pao1_gpl84_gse12678 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null Adenoma, Liver Cell CTD Gene-Disease Associations 1.0 1.06152 growth delay HPO Gene-Disease Associations 1.0 null Ventricular Dysfunction DisGeNET Gene-Phenotype Associations 1.0 null ventriculomegaly HPO Gene-Disease Associations 1.0 null mitochondrion LOCATE Predicted Protein Localization Annotations 1.0 null sudden central visual loss HPO Gene-Disease Associations 1.0 null abnormality of muscle morphology HPO Gene-Disease Associations 1.0 null mode of inheritance HPO Gene-Disease Associations 1.0 null termination GeneRIF Biological Term Annotations 1.0 null protein binding GO Molecular Function Annotations 2015 1.0 null renal insufficiency HPO Gene-Disease Associations 1.0 null PMC9259482-41385_2022_495_MOESM1_ESM.xlsx-S14_neutrophils-Supplemental_Table_13_Neutrophil_cluster1_LPS_vs_LPS_il-1RA_aTNF_IRF6 Rummagene Transcription Factor Associations 2026 1.0 null mRNA_WHSC2_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells 1.0 null Prenatal Exposure Delayed Effects CTD Gene-Disease Associations 1.0 1.85677 PTEN_KD_GDS2958_101_human_SKBR-3 MAMMARY ADENOCARCINOMA cell line GEO Signatures of Differentially Expressed Genes for Gene Perturbations -1.0 null decreased nerve conduction velocity HPO Gene-Disease Associations 1.0 null PMC8493693__F4 PFOCR Pathway Figure Associations 2024 1.0 null sensorineural hearing impairment HPO Gene-Disease Associations 1.0 null congestive heart failure HPO Gene-Disease Associations 1.0 null PMC11385078-jciinsight-9-172336-s272.xlsx-1DEseq2_Report_AA_BL_vs_EA_BL-Unnamed_1_TEAD1 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of nervous system morphology HPO Gene-Disease Associations 1.0 null leigh GeneRIF Biological Term Annotations 1.0 null cellular component organization GO Biological Process Annotations 2015 1.0 null incoordination HPO Gene-Disease Associations 1.0 null abnormality of thyroid physiology HPO Gene-Disease Associations 1.0 null transmembrane transport GO Biological Process Annotations 2015 1.0 null ectopic calcification HPO Gene-Disease Associations 1.0 null Abnormality Of Mitochondrial Metabolism DisGeNET Gene-Phenotype Associations 1.0 null Poisoning CTD Gene-Disease Associations 1.0 1.37532 hsa-miR-320c MiRTarBase microRNA Targets 1.0 null paresthesia HPO Gene-Disease Associations 1.0 null macromolecular complex assembly GO Biological Process Annotations 2015 1.0 null interact GeneRIF Biological Term Annotations 1.0 null Breast Carcinoma DisGeNET Gene-Disease Associations 1.0 null cellular component organization or biogenesis GO Biological Process Annotations 2015 1.0 null Optic Atrophy DisGeNET Gene-Disease Associations 1.0 null PMC3985196-317853.f1.pdf-40-ZNF528_ZNF528 Rummagene Transcription Factor Associations 2026 1.0 null arterial stenosis HPO Gene-Disease Associations 1.0 null abnormality of the retinal pigment epithelium HPO Gene-Disease Associations 1.0 null abnormality of the immune system HPO Gene-Disease Associations 1.0 null clinical modifier HPO Gene-Disease Associations 1.0 null Addison Disease DisGeNET Gene-Disease Associations 1.0 null abnormality of skin pigmentation HPO Gene-Disease Associations 1.0 null single-organism metabolic process GO Biological Process Annotations 2015 1.0 null abnormality of the outer ear HPO Gene-Disease Associations 1.0 null Delayed Puberty DisGeNET Gene-Phenotype Associations 1.0 null transporter activity GO Molecular Function Annotations 2015 1.0 null abnormality of vision HPO Gene-Disease Associations 1.0 null methylprednisolone_rattus norvegicus_gpl85_gds965 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null rhabdomyolysis GeneRIF Biological Term Annotations 1.0 null Aphasia DisGeNET Gene-Disease Associations 1.0 null Cataract DisGeNET Gene-Disease Associations 1.0 null lateral ventricle HPA Tissue Protein Expression Profiles -1.0 -0.772517 Leigh Disease DisGeNET Gene-Disease Associations 1.0 null cisplatin_homo sapiens_gpl570_gse23553 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null family GeneRIF Biological Term Annotations 1.0 null hemiplegia/hemiparesis HPO Gene-Disease Associations 1.0 null PMC11923960-ADVS-12-2411131-s001.pdf-24-DBP_DBP Rummagene Transcription Factor Associations 2026 1.0 null oxidative phosphorylation KEGG Pathways 1.0 null PMC9181267-mmc5.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-hsapiens_homolog_associated_gene_name_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null common GeneRIF Biological Term Annotations 1.0 null severe GeneRIF Biological Term Annotations 1.0 null Generalized Hirsutism DisGeNET Gene-Phenotype Associations 1.0 null GSK3B_knockdown_158_GSE35351 GEO Signatures of Differentially Expressed Genes for Kinase Perturbations -1.0 -1.72899 Hemorrhage CTD Gene-Disease Associations 1.0 1.10699 abnormality of the intestine HPO Gene-Disease Associations 1.0 null PMC7921413-41467_2021_21650_MOESM5_ESM.xlsx-002_DE-CD34_Blasts_AP1_low_JUN Rummagene Transcription Factor Associations 2026 1.0 null abnormal tendon morphology HPO Gene-Disease Associations 1.0 null Drug-Related Side Effects and Adverse Reactions CTD Gene-Disease Associations 1.0 1.10907 hypopigmentation of the skin HPO Gene-Disease Associations 1.0 null abnormality of the cerebellum HPO Gene-Disease Associations 1.0 null upper motor neuron dysfunction HPO Gene-Disease Associations 1.0 null sensory neuropathy HPO Gene-Disease Associations 1.0 null abnormality of vision evoked potentials HPO Gene-Disease Associations 1.0 null abnormality of body weight HPO Gene-Disease Associations 1.0 null Preexcitation Syndrome DisGeNET Gene-Disease Associations 1.0 null abnormality of the pancreas HPO Gene-Disease Associations 1.0 null mtdnaencoded GeneRIF Biological Term Annotations 1.0 null PMC12699144-CTM2-15-e70552-s001.xlsx-T_CD8_c03_ZNF683-Unnamed_0_ZNF683 Rummagene Transcription Factor Associations 2026 1.0 null PMC8212786-DataSheet_4.xlsx-CESC-ZBED3_ZBED3 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of metabolism/homeostasis HPO Gene-Disease Associations 1.0 null PMC11511845-41598_2024_76514_MOESM1_ESM.pdf-13-TCF7L2_TCF7L2 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the posterior segment of the eye HPO Gene-Disease Associations 1.0 null pancreatitis HPO Gene-Disease Associations 1.0 null causing GeneRIF Biological Term Annotations 1.0 null abnormality of the renal tubule HPO Gene-Disease Associations 1.0 null PMC10534007-Table_2.xlsx-S2_overlap_MSC_down_B_V-395_common_elements_in_VM-CUB1_MSC_down_and_BFTC905_MSC_down_MSC Rummagene Transcription Factor Associations 2026 1.0 null abdominal pain HPO Gene-Disease Associations 1.0 null hsa-let-7c-5p MiRTarBase microRNA Targets 1.0 null PMC6345883-41598_2018_37397_MOESM10_ESM.xlsx-AR_D0_VS_D14__TRANS-Gene_Name_AR Rummagene Transcription Factor Associations 2026 1.0 null PMC12337709-mmc3.xlsx-Wild-type_vs_RAG1_KO_spleen-Unnamed_1_RAG1 Rummagene Transcription Factor Associations 2026 1.0 null hypopigmented skin patches HPO Gene-Disease Associations 1.0 null intracellular organelle part GO Cellular Component Annotations 2015 1.0 null abnormality of oral mucosa HPO Gene-Disease Associations 1.0 null amaurosis fugax HPO Gene-Disease Associations 1.0 null Developmental Delay (Disorder) DisGeNET Gene-Phenotype Associations 1.0 null Right Ventricular Hypertrophy DisGeNET Gene-Disease Associations 1.0 null cellular process GO Biological Process Annotations 2015 1.0 null methylprednisolone_rattus norvegicus_gpl85_gds253 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null mRNA_SUZ12_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null Abnormal Vision DisGeNET Gene-Phenotype Associations 1.0 null growth abnormality HPO Gene-Disease Associations 1.0 null PMC10810548-pone.0289518.s002.xlsx-SOM_w_identifiers-target_gene_GRHL3 Rummagene Transcription Factor Associations 2026 1.0 null hsa-miR-744-5p MiRTarBase microRNA Targets 1.0 null total GeneRIF Biological Term Annotations 1.0 null hsa-miR-296-3p MiRTarBase microRNA Targets 1.0 null PMC9181267-mmc5.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-orthofinder_human_gene_names_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null neurological speech impairment HPO Gene-Disease Associations 1.0 null Spontaneous Hematomas DisGeNET Gene-Disease Associations 1.0 null Ophthalmoplegia DisGeNET Gene-Phenotype Associations 1.0 null PMC12375500-41388_2025_3449_MOESM1_ESM.xlsx-DBP_down-gene_DBP Rummagene Transcription Factor Associations 2026 1.0 null Ptosis DisGeNET Gene-Disease Associations 1.0 null cerebral calcification HPO Gene-Disease Associations 1.0 null POT-4 DGIdb Drug Targets 2026 1.0 26.466 monovalent inorganic cation transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null aortic dissection HPO Gene-Disease Associations 1.0 null multiple lipomas HPO Gene-Disease Associations 1.0 null PMC12802643-mmc10.xlsx-EC2-EC2_Endothelial_subcluster_2_TCF15 Rummagene Transcription Factor Associations 2026 1.0 null malabsorption HPO Gene-Disease Associations 1.0 null abnormality of the gingiva HPO Gene-Disease Associations 1.0 null abnormality of the anterior pituitary HPO Gene-Disease Associations 1.0 null Squamous Cell Carcinoma Of The Head And Neck DisGeNET Gene-Disease Associations 1.0 null membrane GO Cellular Component Annotations 2015 1.0 null vitamin c_homo sapiens_gpl570_gds3635 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null Cytochrome c oxidase subunit III domain InterPro Predicted Protein Domain Annotations 1.0 null hsa-miR-186-5p MiRTarBase microRNA Targets 1.0 null PMC4030113__F3 PFOCR Pathway Figure Associations 2024 1.0 null estradiol_homo sapiens_gpl570_gse29881 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null mitochondrial inner membrane GO Cellular Component Annotations 2015 1.0 null PMC12229841-Table2.xlsx-BL_LPS_vs_6mo_LPS-Negative_logFC_up_at_baseline_Postive_logFC_up_after_6mo_of_heavy_drinking_IRF6 Rummagene Transcription Factor Associations 2026 1.0 null Protruding Ear DisGeNET Gene-Phenotype Associations 1.0 null PMC12337709-mmc3.xlsx-Wild-type_vs_RAG1_KO_NK_cells-Unnamed_1_RAG1 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of movement HPO Gene-Disease Associations 1.0 null Hemiparesis DisGeNET Gene-Phenotype Associations 1.0 null greater GeneRIF Biological Term Annotations 1.0 null PMC8101445-mbc-32-475-s003.xlsx-HEK_Tim29_KD-Gene_names_AR Rummagene Transcription Factor Associations 2026 1.0 null alzheimer's disease GAD Gene-Disease Associations 1.0 null mRNA_POU5F1_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null base GeneRIF Biological Term Annotations 1.0 null iii GeneRIF Biological Term Annotations 1.0 null Episodic Vomiting DisGeNET Gene-Phenotype Associations 1.0 null migraine HPO Gene-Disease Associations 1.0 null visual impairment HPO Gene-Disease Associations 1.0 null Acidosis, Lactic DisGeNET Gene-Phenotype Associations 1.0 null Paresthesia DisGeNET Gene-Phenotype Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Macro_DAPI_ERG_VaDadj_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null mtatp6 GeneRIF Biological Term Annotations 1.0 null thickened skin HPO Gene-Disease Associations 1.0 null missense GeneRIF Biological Term Annotations 1.0 null Hepatitis C virus genotype 1b (isolate Con1) Virus MINT Protein-Virus Interactions 1.0 null Adenomatous Polyposis Coli DisGeNET Gene-Disease Associations 1.0 null Disease HuGE Navigator Gene-Phenotype Associations 1.0 null PMC7480058-95058-2020.08.29.20182899-10.xlsx-1ModuleKeyDrivers-Target_gene_symbol_that_KD_acts_upon_AR Rummagene Transcription Factor Associations 2026 1.0 null Retinal Vascular Tortuosity DisGeNET Gene-Phenotype Associations 1.0 null protein complex assembly GO Biological Process Annotations 2015 1.0 null Hypertrophic Cardiomyopathy DisGeNET Gene-Disease Associations 1.0 null abnormality of the skin HPO Gene-Disease Associations 1.0 null PMC5516940__F5 PFOCR Pathway Figure Associations 2024 1.0 null hypercalciuria HPO Gene-Disease Associations 1.0 null abnormality of the cerebral ventricles HPO Gene-Disease Associations 1.0 null alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease GAD Gene-Disease Associations 1.0 null Sodium Azide CTD Gene-Chemical Interactions 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-OLIG2_UNIQUE_DYS_GENES-NEUN_TLE_vs_TL_log2FoldChange_1_padj_0_1_OLIG2 Rummagene Transcription Factor Associations 2026 1.0 null substrate-specific transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null Blepharoptosis DisGeNET Gene-Disease Associations 1.0 null Neoplasms, Experimental CTD Gene-Disease Associations 1.0 1.07732 Weight Loss CTD Gene-Disease Associations 1.0 1.78302 Neoplasms CTD Gene-Disease Associations 1.0 1.06734 transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null monovalent inorganic cation transport GO Biological Process Annotations 2015 1.0 null brain atrophy HPO Gene-Disease Associations 1.0 null organelle membrane GO Cellular Component Annotations 2015 1.0 null PMC9529122-pone.0274785.s002.xlsx-S1_Table-S1A_Table_Differentially_expressed_genes_in_HeyA8_overexpressin_ZNF521_vs_HeyA8_control_cells_ZNF521 Rummagene Transcription Factor Associations 2026 1.0 null atrophy/degeneration affecting the cerebrum HPO Gene-Disease Associations 1.0 null carious teeth HPO Gene-Disease Associations 1.0 null Sudden Cardiac Death DisGeNET Gene-Phenotype Associations 1.0 null abnormality of skeletal morphology HPO Gene-Disease Associations 1.0 null PMC7616765-EMS198548-supplement-Data_S2.xlsx-3_DEG_2D_and_3D-D9_Up_in_3D_CENPX Rummagene Transcription Factor Associations 2026 1.0 null abnormality of joint mobility HPO Gene-Disease Associations 1.0 null abnormality of the parathyroid physiology HPO Gene-Disease Associations 1.0 null visual field defect HPO Gene-Disease Associations 1.0 null PMC12354803-42003_2025_8643_MOESM2_ESM.xlsx-2w_TP63_positive-Gene_TP63 Rummagene Transcription Factor Associations 2026 1.0 null arthrogryposis multiplex congenita HPO Gene-Disease Associations 1.0 null abnormal nerve conduction velocity HPO Gene-Disease Associations 1.0 null morphological abnormality of the central nervous system HPO Gene-Disease Associations 1.0 null abnormality of the eye HPO Gene-Disease Associations 1.0 null oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor GO Molecular Function Annotations 2015 1.0 null cellular_component LOCATE Predicted Protein Localization Annotations 1.0 null respiratory activity following radiotherapy GAD Gene-Disease Associations 1.0 null abnormality of the fundus HPO Gene-Disease Associations 1.0 null abnormality of divalent inorganic cation homeostasis HPO Gene-Disease Associations 1.0 null Dilated Ventricles (Finding) DisGeNET Gene-Phenotype Associations 1.0 null muscle GeneRIF Biological Term Annotations 1.0 null organelle inner membrane GO Cellular Component Annotations 2015 1.0 null neoplasm by anatomical site HPO Gene-Disease Associations 1.0 null SYNCRIP_OE_GDS4596_85_human_SW480 GEO Signatures of Differentially Expressed Genes for Gene Perturbations -1.0 null Cytochrome c oxidase, subunit III, 4-helical bundle InterPro Predicted Protein Domain Annotations 1.0 null hsa-miR-26a-5p MiRTarBase microRNA Targets 1.0 null frame GeneRIF Biological Term Annotations 1.0 null abnormality of the vasculature HPO Gene-Disease Associations 1.0 null Orbital Separation Excessive DisGeNET Gene-Phenotype Associations 1.0 null establishment of localization GO Biological Process Annotations 2015 1.0 null Glomerulopathy Assessment DisGeNET Gene-Phenotype Associations 1.0 null Depression DisGeNET Gene-Disease Associations 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-PAX6_UNIQUE_DYS_GENES-PAX6_TLE_vs_TL_log2FoldChange_1_padj_0_1_PAX6 Rummagene Transcription Factor Associations 2026 1.0 null gastric cancer GAD Gene-Disease Associations 1.0 null Goiter DisGeNET Gene-Phenotype Associations 1.0 null Anxiety DisGeNET Gene-Disease Associations 1.0 null Central Visual Impairment DisGeNET Gene-Disease Associations 1.0 null Fever DisGeNET Gene-Phenotype Associations 1.0 null estradiol_homo sapiens_gpl1225_gse1486 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null vitamin a_rattus norvegicus_gpl85_gse3420 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null cytochrome-c oxidase activity GO Molecular Function Annotations 2015 1.0 null Polyneuropathy DisGeNET Gene-Disease Associations 1.0 null isolated GeneRIF Biological Term Annotations 1.0 null Dwarfism DisGeNET Gene-Disease Associations 1.0 null vincristine_homo sapiens_gpl570_gse7556 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null abnormality of coordination HPO Gene-Disease Associations 1.0 null Respiratory Insufficiency DisGeNET Gene-Phenotype Associations 1.0 null Mask-Like Facies DisGeNET Gene-Phenotype Associations 1.0 null Ragged-Red Muscle Fibers DisGeNET Gene-Phenotype Associations 1.0 null energy derivation by oxidation of organic compounds GO Biological Process Annotations 2015 1.0 null PMC6345883-41598_2018_37397_MOESM10_ESM.xlsx-AR_D0_VS_D7_W_B29__TRANS-Gene_Name_AR Rummagene Transcription Factor Associations 2026 1.0 null ovary HPA Tissue Protein Expression Profiles -1.0 -1.35386 korean GeneRIF Biological Term Annotations 1.0 null intracellular membrane-bounded organelle LOCATE Predicted Protein Localization Annotations 1.0 null abnormal glucose homeostasis HPO Gene-Disease Associations 1.0 null localized skin lesion HPO Gene-Disease Associations 1.0 null abnormality of the metencephalon HPO Gene-Disease Associations 1.0 null Necrosis CTD Gene-Disease Associations 1.0 1.99581 transport GO Biological Process Annotations 2015 1.0 null abnormal hair quantity HPO Gene-Disease Associations 1.0 null Cerebral Ventriculomegaly DisGeNET Gene-Phenotype Associations 1.0 null myopathy GeneRIF Biological Term Annotations 1.0 null Gingival Overgrowth DisGeNET Gene-Phenotype Associations 1.0 null PMC10756545-pone.0296454.s002.xlsx-8_Normal_premalignant_modules-N10_NR4A1 Rummagene Transcription Factor Associations 2026 1.0 null arc GeneRIF Biological Term Annotations 1.0 null Memory Impairment DisGeNET Gene-Phenotype Associations 1.0 null respiratory insufficiency HPO Gene-Disease Associations 1.0 null abnormality of the hair HPO Gene-Disease Associations 1.0 null abnormality of nervous system physiology HPO Gene-Disease Associations 1.0 null PMC6961462-NIHMS1544104-supplement-Sup_Tab.xlsx-Sup_Table_3_a-Supplementary_Table_3_Genes_Regulated_by_A_MYB_in_Humans_and_Macaques_Bold_genes_with_reduced_expression_in_Group_3_MYB Rummagene Transcription Factor Associations 2026 1.0 null cellular metabolic process GO Biological Process Annotations 2015 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-NEUN_UNIQUE_DYS_GENES-PAX6_TLE_vs_TL_log2FoldChange_1_padj_0_1_PAX6 Rummagene Transcription Factor Associations 2026 1.0 null PMC9068765-41467_2022_29960_MOESM14_ESM.xlsx-TP53-Unnamed_2_TP53 Rummagene Transcription Factor Associations 2026 1.0 null Multiple Lipomata DisGeNET Gene-Disease Associations 1.0 null abnormality of the mitochondrion HPO Gene-Disease Associations 1.0 null gastrointestinal obstruction HPO Gene-Disease Associations 1.0 null PMC9588367__F5 PFOCR Pathway Figure Associations 2024 1.0 null hsa-miR-196a-5p MiRTarBase microRNA Targets 1.0 null hyperthyroidism HPO Gene-Disease Associations 1.0 null cytoplasmic part GO Cellular Component Annotations 2015 1.0 null Hypercalciuria DisGeNET Gene-Phenotype Associations 1.0 null Adenocarcinoma CTD Gene-Disease Associations 1.0 1.18882 immediately GeneRIF Biological Term Annotations 1.0 null Visual Impairment DisGeNET Gene-Phenotype Associations 1.0 null PMC7657662__F5 PFOCR Pathway Figure Associations 2024 1.0 null abnormality of the cerebral vasculature HPO Gene-Disease Associations 1.0 null SQSTM1_OE_GDS2653_651_human_IMR-32 neuroblastoma cells GEO Signatures of Differentially Expressed Genes for Gene Perturbations 1.0 null abnormality of the aorta HPO Gene-Disease Associations 1.0 null abnormality of the pinna HPO Gene-Disease Associations 1.0 null bone marrow HPA Tissue Protein Expression Profiles -1.0 -1.35386 abnormality of eye movement HPO Gene-Disease Associations 1.0 null single-organism cellular process GO Biological Process Annotations 2015 1.0 null Cytochrome-C Oxidase Deficiency DisGeNET Gene-Disease Associations 1.0 null inorganic cation transmembrane transport GO Biological Process Annotations 2015 1.0 null pulmonary embolism HPO Gene-Disease Associations 1.0 null encephalomyopathy GeneRIF Biological Term Annotations 1.0 null single-organism transport GO Biological Process Annotations 2015 1.0 null hydrogen transport GO Biological Process Annotations 2015 1.0 null alitretinoin_rattus norvegicus_gpl85_gse3952 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null cognitive ability GAD Gene-Disease Associations 1.0 null abnormality of the lens HPO Gene-Disease Associations 1.0 null Electron transport chain OXPHOS system in mitochondria WikiPathways Pathways 2024 1.0 null large central visual field defect HPO Gene-Disease Associations 1.0 null GSK3B_knockdown_209_GSE35351 GEO Signatures of Differentially Expressed Genes for Kinase Perturbations -1.0 -1.72899 sudden cardiac death HPO Gene-Disease Associations 1.0 null Kidney Diseases CTD Gene-Disease Associations 1.0 1.25651 Fetal Growth Retardation CTD Gene-Disease Associations 1.0 1.35098 doxorubicin_homo sapiens_gpl570_gse46493 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null Left Ventricular Noncompaction Cardiomyopathy DisGeNET Gene-Disease Associations 1.0 null reduced consciousness/confusion HPO Gene-Disease Associations 1.0 null diabetes mellitus HPO Gene-Disease Associations 1.0 null abnormal joint morphology HPO Gene-Disease Associations 1.0 null respiratory electron transport chain GO Biological Process Annotations 2015 1.0 null Autism DisGeNET Gene-Disease Associations 1.0 null abnormality of connective tissue HPO Gene-Disease Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Astro_DAPI_ERG_VaDadj_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null Learning Disorders CTD Gene-Disease Associations 1.0 1.10353 goiter HPO Gene-Disease Associations 1.0 null abnormality of head or neck HPO Gene-Disease Associations 1.0 null Stroke DisGeNET Gene-Phenotype Associations 1.0 null PMC8481886-Table_2.xlsx-A_subsets-AF_MSC_UdRPC_MSC Rummagene Transcription Factor Associations 2026 1.0 null Cytochrome c oxidase subunit III InterPro Predicted Protein Domain Annotations 1.0 null hsa-miR-196b-5p MiRTarBase microRNA Targets 1.0 null hypopituitarism HPO Gene-Disease Associations 1.0 null cell part LOCATE Predicted Protein Localization Annotations 1.0 null hypoparathyroidism HPO Gene-Disease Associations 1.0 null Abnormal Visual Evoked Potential DisGeNET Gene-Phenotype Associations 1.0 null seizures HPO Gene-Disease Associations 1.0 null Epilepsy DisGeNET Gene-Disease Associations 1.0 null abnormality of skeletal physiology HPO Gene-Disease Associations 1.0 null Apnea DisGeNET Gene-Phenotype Associations 1.0 null abnormal retinal pigmentation HPO Gene-Disease Associations 1.0 null cox GeneRIF Biological Term Annotations 1.0 null Optic Atrophy, Hereditary, Leber HuGE Navigator Gene-Phenotype Associations 1.0 null mRNA_MSC_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null PMC11551338-pnas.2411189121.sd01.xlsx-VDR-Unnamed_0_VDR Rummagene Transcription Factor Associations 2026 1.0 null PMC6345883-41598_2018_37397_MOESM10_ESM.xlsx-AR_D0_VS_D7_WO_B29__TRANS-Gene_Name_AR Rummagene Transcription Factor Associations 2026 1.0 null anterior hypopituitarism HPO Gene-Disease Associations 1.0 null PMC6217971__F3 PFOCR Pathway Figure Associations 2024 1.0 null muscular hypotonia HPO Gene-Disease Associations 1.0 null Mitochondrial Respiratory Chain Defects DisGeNET Gene-Phenotype Associations 1.0 null Malignant Tumor Of Colon DisGeNET Gene-Disease Associations 1.0 null electron transport chain GO Biological Process Annotations 2015 1.0 null Hepatomegaly CTD Gene-Disease Associations 1.0 1.37987 Carcinogenesis DisGeNET Gene-Phenotype Associations 1.0 null cardiac arrest HPO Gene-Disease Associations 1.0 null Dental Caries DisGeNET Gene-Disease Associations 1.0 null Nonalcoholic fatty liver disease WikiPathways Pathways 2024 1.0 null cation transport GO Biological Process Annotations 2015 1.0 null eeg abnormality HPO Gene-Disease Associations 1.0 null Mitochondrial Encephalopathy DisGeNET Gene-Disease Associations 1.0 null cognitive impairment HPO Gene-Disease Associations 1.0 null placenta HPA Tissue Protein Expression Profiles 1.0 0.773421 type ii diabetes mellitus HPO Gene-Disease Associations 1.0 null Fatty Liver Disease DisGeNET Gene-Disease Associations 1.0 null Malabsorption DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the systemic arterial tree HPO Gene-Disease Associations 1.0 null estradiol_rattus norvegicus_gpl85_gds2311 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null lipomatous tumor HPO Gene-Disease Associations 1.0 null dna GeneRIF Biological Term Annotations 1.0 null Sensorineural Hearing Loss, Bilateral DisGeNET Gene-Disease Associations 1.0 null Proteinuria DisGeNET Gene-Phenotype Associations 1.0 null abdominal symptom HPO Gene-Disease Associations 1.0 null Blurred Vision, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null reduced tendon reflexes HPO Gene-Disease Associations 1.0 null Dyspnea CTD Gene-Disease Associations 1.0 1.07269 abnormality of carbohydrate metabolism/homeostasis HPO Gene-Disease Associations 1.0 null pathogenicity GeneRIF Biological Term Annotations 1.0 null Tonic - Clonic Seizures DisGeNET Gene-Disease Associations 1.0 null hypertrichosis HPO Gene-Disease Associations 1.0 null cox3 GeneRIF Biological Term Annotations 1.0 null Hyperthyroidism DisGeNET Gene-Disease Associations 1.0 null ganglion GeneRIF Biological Term Annotations 1.0 null oxidoreductase activity, acting on a heme group of donors GO Molecular Function Annotations 2015 1.0 null Micronuclei, Chromosome-Defective CTD Gene-Disease Associations 1.0 1.16467 developmental regression HPO Gene-Disease Associations 1.0 null abnormality of the hypothalamus-pituitary axis HPO Gene-Disease Associations 1.0 null alphasynuclein GeneRIF Biological Term Annotations 1.0 null gefitinib_homo sapiens_gpl570_gse20854 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null PMC11079006-41467_2024_48118_MOESM7_ESM.xlsx-ZNF274_OE_vs_EGFP_CTR_DE-gene_ZNF274 Rummagene Transcription Factor Associations 2026 1.0 null harbor GeneRIF Biological Term Annotations 1.0 null Increased Serum Lactate DisGeNET Gene-Phenotype Associations 1.0 null PMC12824661-BLOOD_BLD-2024-027020-mmc6.xls-Table_S14-HES4_Up_HES4 Rummagene Transcription Factor Associations 2026 1.0 null abnormal pyramidal signs HPO Gene-Disease Associations 1.0 null abnormality of pancreas physiology HPO Gene-Disease Associations 1.0 null oxidoreductase activity GO Molecular Function Annotations 2015 1.0 null abnormality of the optic disc HPO Gene-Disease Associations 1.0 null Abnormal Macular Morphology DisGeNET Gene-Phenotype Associations 1.0 null PMC7936035__F7 PFOCR Pathway Figure Associations 2024 1.0 null Diabetes Mellitus, Type 2 HuGE Navigator Gene-Phenotype Associations 1.0 null Edema CTD Gene-Disease Associations 1.0 1.2639 Reduced Tendon Reflexes DisGeNET Gene-Phenotype Associations 1.0 null major GeneRIF Biological Term Annotations 1.0 null PMC9588367__F8 PFOCR Pathway Figure Associations 2024 1.0 null aerobic electron transport chain GO Biological Process Annotations 2015 1.0 null abnormal bleeding HPO Gene-Disease Associations 1.0 null PMC10350077-media-7.xlsx-Microglia_P_LPS_All_Up_GO-Gene_Symbol_IRF6 Rummagene Transcription Factor Associations 2026 1.0 null neurodevelopmental abnormality HPO Gene-Disease Associations 1.0 null Pancreatitis DisGeNET Gene-Disease Associations 1.0 null cellular protein complex assembly GO Biological Process Annotations 2015 1.0 null tremor HPO Gene-Disease Associations 1.0 null abnormal axial skeleton morphology HPO Gene-Disease Associations 1.0 null Mitochondrial Complex Iv Deficiency DisGeNET Gene-Phenotype Associations 1.0 null proteinuria HPO Gene-Disease Associations 1.0 null Intestinal Obstruction DisGeNET Gene-Disease Associations 1.0 null abnormal peripheral nervous system morphology HPO Gene-Disease Associations 1.0 null small molecule metabolic process GO Biological Process Annotations 2015 1.0 null adrenal insufficiency HPO Gene-Disease Associations 1.0 null PMC9810535-41590_2022_1370_MOESM3_ESM.xlsx-Table_S7-MECOM_up_genes_MECOM Rummagene Transcription Factor Associations 2026 1.0 null Ventricular Preexcitation DisGeNET Gene-Disease Associations 1.0 null premature loss of teeth HPO Gene-Disease Associations 1.0 null Short Stature, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null PMC8101445-mbc-32-475-s003.xlsx-HEK_Tim22_KD-Gene_names_AR Rummagene Transcription Factor Associations 2026 1.0 null feeding difficulties HPO Gene-Disease Associations 1.0 null abnormal facial expression HPO Gene-Disease Associations 1.0 null Anemia CTD Gene-Disease Associations 1.0 1.29966 abnormality of the pulmonary artery HPO Gene-Disease Associations 1.0 null mutant GeneRIF Biological Term Annotations 1.0 null hsa-let-7e-5p MiRTarBase microRNA Targets 1.0 null PMC10800016-table_s3_20230913_ddad186.xlsx-DUX4-aff_II-Unnamed_1_DUX4 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the globe HPO Gene-Disease Associations 1.0 null glomerulopathy HPO Gene-Disease Associations 1.0 null generation of precursor metabolites and energy GO Biological Process Annotations 2015 1.0 null codon GeneRIF Biological Term Annotations 1.0 null abnormality of the genital system HPO Gene-Disease Associations 1.0 null fibers GeneRIF Biological Term Annotations 1.0 null hsa-miR-28-3p MiRTarBase microRNA Targets 1.0 null mRNA_NR5A2_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null congenital contracture HPO Gene-Disease Associations 1.0 null abnormality of the macula HPO Gene-Disease Associations 1.0 null abnormality of the optic nerve HPO Gene-Disease Associations 1.0 null prostate cancer GAD Gene-Disease Associations 1.0 null Congestive Heart Failure DisGeNET Gene-Disease Associations 1.0 null abnormality of the cerebrum HPO Gene-Disease Associations 1.0 null intracellular organelle LOCATE Predicted Protein Localization Annotations 1.0 null binding GO Molecular Function Annotations 2015 1.0 null arrhythmia HPO Gene-Disease Associations 1.0 null number GeneRIF Biological Term Annotations 1.0 null membrane-bounded organelle LOCATE Predicted Protein Localization Annotations 1.0 null PMC4271336-13041_2014_88_MOESM6_ESM.xlsx-Genes_in_GENE_CARD_MR_or_ID-Gene_Cards_MR_and_ID_genes_NR3C2 Rummagene Transcription Factor Associations 2026 1.0 null tunisia GeneRIF Biological Term Annotations 1.0 null Wolff-Parkinson-White Syndrome DisGeNET Gene-Disease Associations 1.0 null sets GeneRIF Biological Term Annotations 1.0 null cardiomyopathy HPO Gene-Disease Associations 1.0 null PMC10830421-41589_2023_1452_MOESM5_ESM.xlsx-HEK293T_MAX-Tg_tissues-Unnamed_0_MAX Rummagene Transcription Factor Associations 2026 1.0 null disorder GeneRIF Biological Term Annotations 1.0 null abnormality of the lung HPO Gene-Disease Associations 1.0 null abnormality of skin adnexa HPO Gene-Disease Associations 1.0 null PMC10313373-jci-133-164637-s072.pdf-18-TERF1_TERF1 Rummagene Transcription Factor Associations 2026 1.0 null Ebolavirus(ZEBOV)_1day_Liver_None_GSE57214 GEO Signatures of Differentially Expressed Genes for Viral Infections 1.0 1.8753 abnormality of the middle ear HPO Gene-Disease Associations 1.0 null Disturbance Of Consciousness DisGeNET Gene-Phenotype Associations 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-OLIG2_UNIQUE_DYS_GENES-OLIG2_TLE_vs_TL_log2FoldChange_1_padj_0_1_OLIG2 Rummagene Transcription Factor Associations 2026 1.0 null Unspecified Visual Loss DisGeNET Gene-Phenotype Associations 1.0 null PMC8721009-Table11.XLSX-Table_S11genes_involved_in_the-TP53_TP53 Rummagene Transcription Factor Associations 2026 1.0 null delayed skeletal maturation HPO Gene-Disease Associations 1.0 null Left Ventricular Hypertrophy DisGeNET Gene-Disease Associations 1.0 null abnormality of cell physiology HPO Gene-Disease Associations 1.0 null Paresthesia CTD Gene-Disease Associations 1.0 1.06771 aerobic respiration GO Biological Process Annotations 2015 1.0 null Variable Expressivity DisGeNET Gene-Phenotype Associations 1.0 null flexion contracture HPO Gene-Disease Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Macro_DAPI_ERG_VaD_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null soft tissue HPA Tissue Protein Expression Profiles -1.0 -0.970296 abnormality of forebrain morphology HPO Gene-Disease Associations 1.0 null Mitochondrial Diabetes DisGeNET Gene-Disease Associations 1.0 null ion transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null aplasia/hypoplasia of the cerebellum HPO Gene-Disease Associations 1.0 null Alzheimer Disease DisGeNET Gene-Disease Associations 1.0 null abnormality of skin morphology HPO Gene-Disease Associations 1.0 null Cognition Disorders CTD Gene-Disease Associations 1.0 1.04389 Hyperplasia CTD Gene-Disease Associations 1.0 1.36791 nucleotide GeneRIF Biological Term Annotations 1.0 null PMC2148057__F5 PFOCR Pathway Figure Associations 2024 1.0 null PMC11630641-mmc8.xlsx-Human_1000cell_NOT_identified-Unnamed_1_NR4A2 Rummagene Transcription Factor Associations 2026 1.0 null mitochondrial part GO Cellular Component Annotations 2015 1.0 null abnormality of the respiratory system HPO Gene-Disease Associations 1.0 null Hypertension CTD Gene-Disease Associations 1.0 1.03715 Hallucinations DisGeNET Gene-Disease Associations 1.0 null Q9WMX2 Virus MINT Protein-Viral Protein Interactions 1.0 null spontaneous hematomas HPO Gene-Disease Associations 1.0 null esophagus HPA Tissue Protein Expression Profiles 1.0 1.41647 PMC12699144-CTM2-15-e70552-s001.xlsx-T_CD4_c02_FOS-Unnamed_0_FOS Rummagene Transcription Factor Associations 2026 1.0 null PMC11814291-41698_2025_830_MOESM1_ESM.pdf-3-ASCL1_ASCL1 Rummagene Transcription Factor Associations 2026 1.0 null Central Retinal Vessel Vascular Tortuosity DisGeNET Gene-Phenotype Associations 1.0 null PMC11960529-mmc4.xlsx-Atrial_LHX2_KOoverCT-gene_LHX2 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of mitochondrial metabolism HPO Gene-Disease Associations 1.0 null Dementia DisGeNET Gene-Disease Associations 1.0 null liver HPA Tissue Protein Expression Profiles -1.0 -1.35386 confers GeneRIF Biological Term Annotations 1.0 null cerebral atrophy HPO Gene-Disease Associations 1.0 null hydrogen ion transmembrane transport GO Biological Process Annotations 2015 1.0 null Feeding Difficulties In Infancy DisGeNET Gene-Phenotype Associations 1.0 null PMC12816669-41698_2025_1236_MOESM1_ESM.pdf-823-DDIT3_DDIT3 Rummagene Transcription Factor Associations 2026 1.0 null single-organism process GO Biological Process Annotations 2015 1.0 null abnormality of temperature regulation HPO Gene-Disease Associations 1.0 null abnormality of body height HPO Gene-Disease Associations 1.0 null alitretinoin_rattus norvegicus_gpl85_liver b_gds2385 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null abnormality of muscle size HPO Gene-Disease Associations 1.0 null brain very small HPO Gene-Disease Associations 1.0 null Diabetes DisGeNET Gene-Disease Associations 1.0 null abnormality of the mouth HPO Gene-Disease Associations 1.0 null asthenospermic GeneRIF Biological Term Annotations 1.0 null abnormality of the urinary system HPO Gene-Disease Associations 1.0 null emg abnormality HPO Gene-Disease Associations 1.0 null epidermal thickening HPO Gene-Disease Associations 1.0 null Malabsorption, Ctcae DisGeNET Gene-Phenotype Associations 1.0 null PMC9590125-40478_2022_1453_MOESM3_ESM.xlsx-PAX6_UNIQUE_DYS_GENES-NEUN_TLE_vs_TL_log2FoldChange_1_padj_0_1_PAX6 Rummagene Transcription Factor Associations 2026 1.0 null hsa-miR-320a MiRTarBase microRNA Targets 1.0 null single GeneRIF Biological Term Annotations 1.0 null biological_process GO Biological Process Annotations 2015 1.0 null Blurred Vision DisGeNET Gene-Phenotype Associations 1.0 null FGFR3_KD_GDS4454_78_human_RT112 GEO Signatures of Differentially Expressed Genes for Gene Perturbations 1.0 null skeletal muscle atrophy HPO Gene-Disease Associations 1.0 null PMC9181267-mmc5.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-GSEA_name_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null PMC12868900-41467_2025_68060_MOESM1_ESM.pdf-4-IKZF2_IKZF2 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the adrenal glands HPO Gene-Disease Associations 1.0 null PMC7000220-elife-50163-fig3-data1.xlsx-genes_SOM_xls-gene_symbol_GRHL3 Rummagene Transcription Factor Associations 2026 1.0 null hsa-let-7b-5p MiRTarBase microRNA Targets 1.0 null hypertelorism HPO Gene-Disease Associations 1.0 null behavioral abnormality HPO Gene-Disease Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Astro_DAPI_ERG_VaD_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null spleen HPA Tissue Protein Expression Profiles -1.0 -1.35386 molecular_function GO Molecular Function Annotations 2015 1.0 null myalgia HPO Gene-Disease Associations 1.0 null Psychotic Episodes DisGeNET Gene-Disease Associations 1.0 null aplasia/hypoplasia involving the central nervous system HPO Gene-Disease Associations 1.0 null abnormality of skeletal maturation HPO Gene-Disease Associations 1.0 null Lung Neoplasms CTD Gene-Disease Associations 1.0 1.17366 Genetic Recurrent Myoglobinuria DisGeNET Gene-Disease Associations 1.0 null cerebral ischemia HPO Gene-Disease Associations 1.0 null ion transmembrane transport GO Biological Process Annotations 2015 1.0 null PMC9218776-ADVS-9-2104640-s002.xlsx-SIM_-_Nurr1-Unnamed_1_SIM2 Rummagene Transcription Factor Associations 2026 1.0 null neuromuscular GeneRIF Biological Term Annotations 1.0 null Enterovirus 71_4Hour_None_GSE15323 GEO Signatures of Differentially Expressed Genes for Viral Infections -1.0 -1.25104 PMC9399107-41467_2022_32627_MOESM6_ESM.xlsx-20_T-cell_subsets-gene_name_CD8_C1_LEF1_LEF1 Rummagene Transcription Factor Associations 2026 1.0 null Hypopigmented Skin Patch DisGeNET Gene-Phenotype Associations 1.0 null enzyme GeneRIF Biological Term Annotations 1.0 null PMC11585558-41467_2024_54547_MOESM8_ESM.xlsx-TP53_vs_WT_DEG_FFPE-gene_name_TP53 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of hindbrain morphology HPO Gene-Disease Associations 1.0 null integral component of membrane GO Cellular Component Annotations 2015 1.0 null Cadmium CTD Gene-Chemical Interactions 1.0 null optic disc pallor HPO Gene-Disease Associations 1.0 null functional abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null Abnormal Aortic Valve Physiology DisGeNET Gene-Disease Associations 1.0 null oxidation-reduction process GO Biological Process Annotations 2015 1.0 null intracellular part GO Cellular Component Annotations 2015 1.0 null substrate-specific transporter activity GO Molecular Function Annotations 2015 1.0 null azithromycin_pseudomonas aeruginosa_gpl84_gse12738 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null Muscle Weakness DisGeNET Gene-Phenotype Associations 1.0 null abnormal renal morphology HPO Gene-Disease Associations 1.0 null Hypoparathyroidism DisGeNET Gene-Disease Associations 1.0 null Microcephaly DisGeNET Gene-Disease Associations 1.0 null constipation HPO Gene-Disease Associations 1.0 null hypertrophic cardiomyopathy HPO Gene-Disease Associations 1.0 null Cerebral Ischemia DisGeNET Gene-Disease Associations 1.0 null PMC12337709-mmc3.xlsx-Wild-type_vs_RAG1_KO_Myeloid-Unnamed_1_RAG1 Rummagene Transcription Factor Associations 2026 1.0 null hypertension HPO Gene-Disease Associations 1.0 null gemcitabine CTD Gene-Chemical Interactions 1.0 null abnormality of cardiovascular system physiology HPO Gene-Disease Associations 1.0 null lymph node HPA Tissue Protein Expression Profiles -1.0 -1.35386 Cardiac Arrhythmia DisGeNET Gene-Phenotype Associations 1.0 null Liver Failure CTD Gene-Disease Associations 1.0 1.01137 feeding difficulties in infancy HPO Gene-Disease Associations 1.0 null memory impairment HPO Gene-Disease Associations 1.0 null heteroplasmic GeneRIF Biological Term Annotations 1.0 null abnormality of the head HPO Gene-Disease Associations 1.0 null abnormality of cardiac morphology HPO Gene-Disease Associations 1.0 null ptosis HPO Gene-Disease Associations 1.0 null Retinal Telangiectasia DisGeNET Gene-Disease Associations 1.0 null Slow Decrease In Visual Acuity DisGeNET Gene-Phenotype Associations 1.0 null PMC7003708__F1 PFOCR Pathway Figure Associations 2023 1.0 null Breast Neoplasms HuGE Navigator Gene-Phenotype Associations 1.0 null protein complex GO Cellular Component Annotations 2015 1.0 null Cortical Visual Impairment DisGeNET Gene-Phenotype Associations 1.0 null PMC5133671__F8 PFOCR Pathway Figure Associations 2024 1.0 null abnormalities of the peripheral arteries HPO Gene-Disease Associations 1.0 null Thyroiditis DisGeNET Gene-Disease Associations 1.0 null PMC7789003__F1 PFOCR Pathway Figure Associations 2024 1.0 null abnormality of skull size HPO Gene-Disease Associations 1.0 null neoplasm of fatty tissue HPO Gene-Disease Associations 1.0 null Malaria DisGeNET Gene-Disease Associations 1.0 null Arthrogryposis DisGeNET Gene-Disease Associations 1.0 null PEGCETACOPLAN DGIdb Drug Targets 2026 1.0 13.233 PMC7899164__F6 PFOCR Pathway Figure Associations 2024 1.0 null deletion GeneRIF Biological Term Annotations 1.0 null Electron Transport Chain(Mus musculus) WikiPathways Pathways 2014 1.0 null organelle LOCATE Predicted Protein Localization Annotations 1.0 null anorexia HPO Gene-Disease Associations 1.0 null abnormality of urine homeostasis HPO Gene-Disease Associations 1.0 null PMC12520974-44161_2025_709_MOESM2_ESM.xlsx-Extended_Data_Fig_4a-Extended_Data_Fig_4a_Marker_genes_used_in_the_heatmap_for_ATF3_4_Capillary_and_Venous_in_non-ischemic_vs_PAD_comparison_ATF3 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the upper urinary tract HPO Gene-Disease Associations 1.0 null Tremor DisGeNET Gene-Phenotype Associations 1.0 null tamoxifen_homo sapiens_gpl570_gds4095 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null macromolecular complex GO Cellular Component Annotations 2015 1.0 null pregnancy loss GAD Gene-Disease Associations 1.0 null Liver Neoplasms CTD Gene-Disease Associations 1.0 1.54693 pair GeneRIF Biological Term Annotations 1.0 null nephrotic syndrome HPO Gene-Disease Associations 1.0 null aplasia/hypoplasia of the cerebrum HPO Gene-Disease Associations 1.0 null Delayed Bone Age DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the nervous system HPO Gene-Disease Associations 1.0 null Hepatitis B DisGeNET Gene-Disease Associations 1.0 null abnormality of the abdomen HPO Gene-Disease Associations 1.0 null abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null Carcinoma, Papillary DisGeNET Gene-Disease Associations 1.0 null syndrome GeneRIF Biological Term Annotations 1.0 null PMC8554124-DataSheet2.XLSX-34-RFX3_RFX3 Rummagene Transcription Factor Associations 2026 1.0 null Electromyogram Abnormal DisGeNET Gene-Phenotype Associations 1.0 null PMC9181267-mmc3.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-GSEA_name_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null PMC12048643-44318_2025_409_MOESM3_ESM.xlsx-HAND1_neg_targets-Gene_HAND1 Rummagene Transcription Factor Associations 2026 1.0 null Gastroparesis DisGeNET Gene-Disease Associations 1.0 null Blindness CTD Gene-Disease Associations 1.0 1.10424 Idiopathic Pulmonary Arterial Hypertension DisGeNET Gene-Disease Associations 1.0 null mechanism of acetaminophen activity and toxicity Biocarta Pathways 1.0 null organelle part GO Cellular Component Annotations 2015 1.0 null autistic behavior HPO Gene-Disease Associations 1.0 null PMC10201771-12864_2023_9385_MOESM1_ESM.xlsx-ST18-Unnamed_11_ST18 Rummagene Transcription Factor Associations 2026 1.0 null Liver Neoplasms, Experimental CTD Gene-Disease Associations 1.0 1.12668 abnormality of peripheral nervous system electrophysiology HPO Gene-Disease Associations 1.0 null intestinal obstruction HPO Gene-Disease Associations 1.0 null vascular skin abnormality HPO Gene-Disease Associations 1.0 null papilledema HPO Gene-Disease Associations 1.0 null abnormal eye morphology HPO Gene-Disease Associations 1.0 null gingival overgrowth HPO Gene-Disease Associations 1.0 null mtdna GeneRIF Biological Term Annotations 1.0 null Childhood Acute Lymphoblastic Leukemia DisGeNET Gene-Disease Associations 1.0 null proton transport GO Biological Process Annotations 2015 1.0 null subunit GeneRIF Biological Term Annotations 1.0 null abnormality of dental structure HPO Gene-Disease Associations 1.0 null PMC7617064-EMS151900-supplement-Extended_Data_Figure_7_Source_Data.xlsx-D23_RORC-Logfold_change_threshold_1_0_1_RORC Rummagene Transcription Factor Associations 2026 1.0 null Cerebral Calcification DisGeNET Gene-Phenotype Associations 1.0 null functional respiratory abnormality HPO Gene-Disease Associations 1.0 null Colorectal Neoplasms HuGE Navigator Gene-Phenotype Associations 1.0 null Nyctalopia DisGeNET Gene-Disease Associations 1.0 null thyroiditis HPO Gene-Disease Associations 1.0 null mRNA_CDX2_19796622 ESCAPE Omics Signatures of Genes and Proteins for Stem Cells -1.0 null intracellular part LOCATE Predicted Protein Localization Annotations 1.0 null abnormality of peripheral nerve conduction HPO Gene-Disease Associations 1.0 null abnormality of cerebral artery HPO Gene-Disease Associations 1.0 null Mitochondrial complex IV assembly WikiPathways Pathways 2024 1.0 null than GeneRIF Biological Term Annotations 1.0 null ovarian cancer GAD Gene-Disease Associations 1.0 null Cachexia DisGeNET Gene-Phenotype Associations 1.0 null oxidase GeneRIF Biological Term Annotations 1.0 null PMC8385445__F1 PFOCR Pathway Figure Associations 2024 1.0 null macromolecular complex subunit organization GO Biological Process Annotations 2015 1.0 null Dystonia DisGeNET Gene-Phenotype Associations 1.0 null cytochrome complex GO Cellular Component Annotations 2015 1.0 null abnormality of brain morphology HPO Gene-Disease Associations 1.0 null Static Tremor DisGeNET Gene-Phenotype Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Mic_DAPI_ERG_VaDadj_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the skull HPO Gene-Disease Associations 1.0 null abnormality of urine calcium concentration HPO Gene-Disease Associations 1.0 null Scotoma DisGeNET Gene-Phenotype Associations 1.0 null hyperactivity HPO Gene-Disease Associations 1.0 null Parkinson Disease HuGE Navigator Gene-Phenotype Associations 1.0 null cytochrome complex assembly GO Biological Process Annotations 2015 1.0 null abnormality of the nephron HPO Gene-Disease Associations 1.0 null hypothyroidism HPO Gene-Disease Associations 1.0 null PMC12699144-CTM2-15-e70552-s001.xlsx-T_CD4_c03_ANXA2_FOXP3-Unnamed_0_FOXP3 Rummagene Transcription Factor Associations 2026 1.0 null mtco3 GeneRIF Biological Term Annotations 1.0 null hearing impairment HPO Gene-Disease Associations 1.0 null specifically GeneRIF Biological Term Annotations 1.0 null abnormality of muscle physiology HPO Gene-Disease Associations 1.0 null abnormality of higher mental function HPO Gene-Disease Associations 1.0 null Hypertrophy CTD Gene-Disease Associations 1.0 1.43755 weakness due to upper motor neuron dysfunction HPO Gene-Disease Associations 1.0 null Myalgia DisGeNET Gene-Phenotype Associations 1.0 null melas GeneRIF Biological Term Annotations 1.0 null abnormality of the ocular region HPO Gene-Disease Associations 1.0 null hearing abnormality HPO Gene-Disease Associations 1.0 null Short Stature DisGeNET Gene-Phenotype Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Neu_DAPI_ERG_VaD_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null PMC11409756-13062_2024_533_MOESM1_ESM.xlsx-Sheet1-Table_S1_Differentially_expressed_genes_DEGs_regulated_by_ZFP64_through_mRNA-seq_ZFP64 Rummagene Transcription Factor Associations 2026 1.0 null PMC3294166__F8 PFOCR Pathway Figure Associations 2024 1.0 null abnormal respiratory system morphology HPO Gene-Disease Associations 1.0 null electron carrier activity GO Molecular Function Annotations 2015 1.0 null autism HPO Gene-Disease Associations 1.0 null ribavirin_homo sapiens_gpl570_gds4391 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null malformation of the heart and great vessels HPO Gene-Disease Associations 1.0 null Breast Neoplasms CTD Gene-Disease Associations 1.0 1.20196 PMC6781638__F4 PFOCR Pathway Figure Associations 2023 1.0 null PMC9181267-mmc3.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-hsapiens_homolog_associated_gene_name_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null TYK2_KD_GDS4754_158_human_JURKAT GEO Signatures of Differentially Expressed Genes for Gene Perturbations 1.0 null Aortic Aneurysm DisGeNET Gene-Disease Associations 1.0 null inorganic cation transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null Abnormality Of Retinal Pigmentation DisGeNET Gene-Phenotype Associations 1.0 null estradiol_homo sapiens_gpl570_gse16683 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null Ataxia DisGeNET Gene-Phenotype Associations 1.0 null PMC11925450-elife-96850-supp2.xlsx-DNMT1_KO_vs_DNMT1_L1TD1_dKO_res-geneName_DNMT1 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of neuronal migration HPO Gene-Disease Associations 1.0 null Ophthalmoparesis DisGeNET Gene-Phenotype Associations 1.0 null cell part GO Cellular Component Annotations 2015 1.0 null PMC12103066-FEBS-292-2688-s001.pdf-36-ZNF107_ZNF107 Rummagene Transcription Factor Associations 2026 1.0 null mitochondrial inheritance HPO Gene-Disease Associations 1.0 null night blindness HPO Gene-Disease Associations 1.0 null Inflammation CTD Gene-Disease Associations 1.0 1.51105 abnormal eye physiology HPO Gene-Disease Associations 1.0 null pof - premature ovarian failure; primary ovarian insufficiency GAD Gene-Disease Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Oligo_DAPI_ERG_VaD_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null Bilateral Cataracts (Disorder) DisGeNET Gene-Disease Associations 1.0 null Muscle Hypotonia DisGeNET Gene-Phenotype Associations 1.0 null abnormality of the pituitary gland HPO Gene-Disease Associations 1.0 null STAT1_KD_GDS4754_159_human_JURKAT GEO Signatures of Differentially Expressed Genes for Gene Perturbations -1.0 null hallucinations HPO Gene-Disease Associations 1.0 null subcutaneous hemorrhage HPO Gene-Disease Associations 1.0 null Electroencephalogram Abnormal DisGeNET Gene-Phenotype Associations 1.0 null cellular respiration GO Biological Process Annotations 2015 1.0 null cytoplasmic part LOCATE Predicted Protein Localization Annotations 1.0 null abnormality of the face HPO Gene-Disease Associations 1.0 null ophthalmoparesis HPO Gene-Disease Associations 1.0 null Nausea And Vomiting DisGeNET Gene-Phenotype Associations 1.0 null abnormality of cation homeostasis HPO Gene-Disease Associations 1.0 null Creatine Phosphokinase Serum Increased DisGeNET Gene-Phenotype Associations 1.0 null Memory Disorders CTD Gene-Disease Associations 1.0 1.28827 Uncinate Epilepsy DisGeNET Gene-Disease Associations 1.0 null Diabetes Mellitus DisGeNET Gene-Disease Associations 1.0 null parathyroid gland HPA Tissue Protein Expression Profiles 1.0 1.41647 Zalcitabine CTD Gene-Chemical Interactions 1.0 null Ataxia HuGE Navigator Gene-Phenotype Associations 1.0 null neoplasm HPO Gene-Disease Associations 1.0 null Liver Carcinoma DisGeNET Gene-Disease Associations 1.0 null Fatigue DisGeNET Gene-Phenotype Associations 1.0 null mitochondrial GeneRIF Biological Term Annotations 1.0 null rosiglitazone_homo sapiens_gpl570_gds2453 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null PMC8995879-Table_1.xlsx-exome_variants_MAF_0_01-Gencode_34_hugoSymbol_MAF Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the endocrine system HPO Gene-Disease Associations 1.0 null functional abnormality of the inner ear HPO Gene-Disease Associations 1.0 null abnormality of the abdominal organs HPO Gene-Disease Associations 1.0 null oral mucosa HPA Tissue Protein Expression Profiles 1.0 1.41647 PMC10803041-elife-86204-supp2.xlsx-scRNA-seq_Snc-KD_in_HT-gene_name_AR Rummagene Transcription Factor Associations 2026 1.0 null intrinsic component of membrane GO Cellular Component Annotations 2015 1.0 null vagina HPA Tissue Protein Expression Profiles 1.0 1.41647 abnormality of the retina HPO Gene-Disease Associations 1.0 null decreased facial expression HPO Gene-Disease Associations 1.0 null PMC11073972-41375_2024_2232_MOESM2_ESM.xlsx-REL-14_CD7_CD1a-_L-IC_DEG-DEG_L2FC_1_0_FDR_0_05_REL Rummagene Transcription Factor Associations 2026 1.0 null aortic dilatation HPO Gene-Disease Associations 1.0 null Death In Early Adulthood DisGeNET Gene-Phenotype Associations 1.0 null atrophy/degeneration affecting the central nervous system HPO Gene-Disease Associations 1.0 null elevated pulmonary artery pressure HPO Gene-Disease Associations 1.0 null Melas Syndrome DisGeNET Gene-Disease Associations 1.0 null estradiol_homo sapiens_gpl570_gse5102 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null mask-like facies HPO Gene-Disease Associations 1.0 null abnormality of central nervous system electrophysiology HPO Gene-Disease Associations 1.0 null membrane part GO Cellular Component Annotations 2015 1.0 null Low Tension Glaucoma HuGE Navigator Gene-Phenotype Associations 1.0 null abnormality of the thyroid gland HPO Gene-Disease Associations 1.0 null short attention span HPO Gene-Disease Associations 1.0 null abnormality of the orbital region HPO Gene-Disease Associations 1.0 null cytochrome GeneRIF Biological Term Annotations 1.0 null abnormality of the inner ear HPO Gene-Disease Associations 1.0 null Dysarthria DisGeNET Gene-Disease Associations 1.0 null Epilepsy, Temporal Lobe CTD Gene-Disease Associations 1.0 2.88009 Developmental Regression DisGeNET Gene-Disease Associations 1.0 null Tubulointerstitial Abnormality DisGeNET Gene-Disease Associations 1.0 null phenotypic abnormality HPO Gene-Disease Associations 1.0 null abnormality of the integument HPO Gene-Disease Associations 1.0 null Glaucoma, Open-Angle HuGE Navigator Gene-Phenotype Associations 1.0 null PMC11426526-ppat.1012555.s014.xlsx-DEG_DC_C91-PL_LPS_vs_DC_Jurkat-DEG_MDDC_C91-PL_LPS_vs_MDDC_Jurkat_IRF6 Rummagene Transcription Factor Associations 2026 1.0 null Obesity HuGE Navigator Gene-Phenotype Associations 1.0 null Attention Deficit Disorder DisGeNET Gene-Disease Associations 1.0 null all HPO Gene-Disease Associations 1.0 null Familial (Fpah) DisGeNET Gene-Disease Associations 1.0 null PMC11799530-12276_2024_1380_MOESM1_ESM.xlsx-DEG_KD_PC-Symbol_AR Rummagene Transcription Factor Associations 2026 1.0 null PMC10172325-41598_2023_34728_MOESM5_ESM.xlsx-KD_Upregulated-Unnamed_7_AR Rummagene Transcription Factor Associations 2026 1.0 null abnormal pattern of respiration HPO Gene-Disease Associations 1.0 null Neurotoxicity Syndromes CTD Gene-Disease Associations 1.0 1.25463 localization GO Biological Process Annotations 2015 1.0 null cellular macromolecular complex assembly GO Biological Process Annotations 2015 1.0 null abnormality of the liver HPO Gene-Disease Associations 1.0 null muscle weakness HPO Gene-Disease Associations 1.0 null Colon Carcinoma DisGeNET Gene-Disease Associations 1.0 null abnormality of the skeletal system HPO Gene-Disease Associations 1.0 null abnormality of the glomerulus HPO Gene-Disease Associations 1.0 null abnormality of adipose tissue HPO Gene-Disease Associations 1.0 null abnormality of the teeth HPO Gene-Disease Associations 1.0 null Anorexia DisGeNET Gene-Disease Associations 1.0 null PMC6928094-395_2019_765_MOESM7_ESM.xls-DEGs_AR7_vs_Pre-patterned-List_of_differentially_expressed_genes_in_AR7_vs_Pre-patterned_cells_THRA Rummagene Transcription Factor Associations 2026 1.0 null single-organism localization GO Biological Process Annotations 2015 1.0 null PTPN1_KD_GSE54157_673_human_KM-H2 GEO Signatures of Differentially Expressed Genes for Gene Perturbations -1.0 null involuntary movements HPO Gene-Disease Associations 1.0 null vitamin a_rattus norvegicus_gpl85_gds238 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null abnormality of thyroid morphology HPO Gene-Disease Associations 1.0 null attention deficit hyperactivity disorder HPO Gene-Disease Associations 1.0 null Electron Transport Chain(Homo sapiens) WikiPathways Pathways 2014 1.0 null patient GeneRIF Biological Term Annotations 1.0 null FGFR3_KD_GDS4454_79_human_RT112 GEO Signatures of Differentially Expressed Genes for Gene Perturbations 1.0 null PMC4918724__F5 PFOCR Pathway Figure Associations 2024 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Oligo_DAPI_ERG_VaDadj_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null primary adrenal insufficiency HPO Gene-Disease Associations 1.0 null cataract HPO Gene-Disease Associations 1.0 null abnormality of the ear HPO Gene-Disease Associations 1.0 null abnormality of the oral cavity HPO Gene-Disease Associations 1.0 null Decreased Nerve Conduction Velocity DisGeNET Gene-Phenotype Associations 1.0 null Cerebral Cortical Atrophy DisGeNET Gene-Disease Associations 1.0 null abnormality of immune system physiology HPO Gene-Disease Associations 1.0 null abnormality of the myocardium HPO Gene-Disease Associations 1.0 null short stature HPO Gene-Disease Associations 1.0 null inorganic ion transmembrane transport GO Biological Process Annotations 2015 1.0 null abnormality of the pulmonary vasculature HPO Gene-Disease Associations 1.0 null pulmonary hypertension HPO Gene-Disease Associations 1.0 null alitretinoin_rattus norvegicus_gpl85_lung_gds2385 GEO Signatures of Differentially Expressed Genes for Small Molecules -1.0 null onset HPO Gene-Disease Associations 1.0 null PMC9181267-mmc3.xls-FILTERED_OLD-INFvsYOUNG-INF_LUN-orthofinder_human_gene_names_TOPORS Rummagene Transcription Factor Associations 2026 1.0 null abnormal renal physiology HPO Gene-Disease Associations 1.0 null SARS-CoV MA15_Day4-PFU-10^4_None_GSE33266 GEO Signatures of Differentially Expressed Genes for Viral Infections -1.0 -1.79769 PMC9810535-41590_2022_1370_MOESM3_ESM.xlsx-Table_S3-MECOM_up_genes_MECOM Rummagene Transcription Factor Associations 2026 1.0 null cation transmembrane transport GO Biological Process Annotations 2015 1.0 null Amaurosis DisGeNET Gene-Phenotype Associations 1.0 null cellular_component GO Cellular Component Annotations 2015 1.0 null SNAI1_OE_GDS4596_344_human_SW480 - Colorectal cancer cell line GEO Signatures of Differentially Expressed Genes for Gene Perturbations 1.0 null optic atrophy HPO Gene-Disease Associations 1.0 null abnormality of calcium homeostasis HPO Gene-Disease Associations 1.0 null Aplasia/Hypoplasia Of The Cerebellum DisGeNET Gene-Phenotype Associations 1.0 null Dissection Of Aorta DisGeNET Gene-Disease Associations 1.0 null homoplasmic GeneRIF Biological Term Annotations 1.0 null Growth Abnormality DisGeNET Gene-Phenotype Associations 1.0 null nausea and vomiting HPO Gene-Disease Associations 1.0 null PMC12064718-41467_2025_59457_MOESM3_ESM.xlsx-LLPS-aboriginal_proteins-ZNF546_ZNF546 Rummagene Transcription Factor Associations 2026 1.0 null cation transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null PMC11166884-mmc4.xlsx-Table_S3-Table_S3_proinflammatory-EC2_comparison_between_WT_and_TG_TCF15 Rummagene Transcription Factor Associations 2026 1.0 null 5q35 copy number variation WikiPathways Pathways 2024 1.0 null metabolic process GO Biological Process Annotations 2015 1.0 null abnormality of adrenal physiology HPO Gene-Disease Associations 1.0 null Abdominal Pain DisGeNET Gene-Phenotype Associations 1.0 null Renal Insufficiency DisGeNET Gene-Disease Associations 1.0 null Forgetful DisGeNET Gene-Phenotype Associations 1.0 null PMC9170821-JCMM-26-3183-s001.xlsx-Neu_DAPI_ERG_VaDadj_vs_NC-Gene_ERG Rummagene Transcription Factor Associations 2026 1.0 null PMC11960529-mmc4.xlsx-Ventricular_ZNF711_KOoverCT-gene_ZNF711 Rummagene Transcription Factor Associations 2026 1.0 null peripheral neuropathy HPO Gene-Disease Associations 1.0 null mitochondrial membrane GO Cellular Component Annotations 2015 1.0 null hsa-miR-484 MiRTarBase microRNA Targets 1.0 null respiratory chain complex iv GO Cellular Component Annotations 2015 1.0 null hydrogen ion transmembrane transporter activity GO Molecular Function Annotations 2015 1.0 null decreased body weight HPO Gene-Disease Associations 1.0 null heme-copper terminal oxidase activity GO Molecular Function Annotations 2015 1.0 null normal GeneRIF Biological Term Annotations 1.0 null Heart Diseases CTD Gene-Disease Associations 1.0 1.36104 Malformations Of Cortical Development DisGeNET Gene-Disease Associations 1.0 null ion transport GO Biological Process Annotations 2015 1.0 null morphological abnormality of the gastrointestinal tract HPO Gene-Disease Associations 1.0 null Icthyosis DisGeNET Gene-Disease Associations 1.0 null Sensorineural Hearing Loss (Disorder) DisGeNET Gene-Disease Associations 1.0 null history GeneRIF Biological Term Annotations 1.0 null catalytic activity GO Molecular Function Annotations 2015 1.0 null abnormality of ion homeostasis HPO Gene-Disease Associations 1.0 null abnormality of the cardiovascular system HPO Gene-Disease Associations 1.0 null abnormal nervous system electrophysiology HPO Gene-Disease Associations 1.0 null Mitochondrial Myopathy DisGeNET Gene-Disease Associations 1.0 null Heart Block DisGeNET Gene-Disease Associations 1.0 null abnormality of the kidney HPO Gene-Disease Associations 1.0 null abnormality of the genitourinary system HPO Gene-Disease Associations 1.0 null oxandrolone_homo sapiens_gpl97_gds1334 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null level GeneRIF Biological Term Annotations 1.0 null abnormal muscle tone HPO Gene-Disease Associations 1.0 null Anterior Hypopituitarism DisGeNET Gene-Disease Associations 1.0 null type i diabetes mellitus HPO Gene-Disease Associations 1.0 null PMC8410861-41467_2021_25544_MOESM32_ESM.xlsx-MCR-MCR_cells_-_DGE_iGCA_testis_vs_adult_testis_from_GSE112013_and_GSE124263_NR3C2 Rummagene Transcription Factor Associations 2026 1.0 null salivary gland HPA Tissue Protein Expression Profiles 1.0 1.41647 abnormality of the urinary system physiology HPO Gene-Disease Associations 1.0 null PMC9399107-41467_2022_32627_MOESM6_ESM.xlsx-7_B-cell_subsets-gene_name_Bcell_C5_NR4A1_NR4A1 Rummagene Transcription Factor Associations 2026 1.0 null abnormality of the anterior segment of the eye HPO Gene-Disease Associations 1.0 null abnormality of the musculature HPO Gene-Disease Associations 1.0 null PMC12586484-41598_2025_22484_MOESM2_ESM.xlsx-Supplementary_Table_1-Supplementary_Table_1_DEGs_in_ATOH8-depleted_EVT_ATOH8 Rummagene Transcription Factor Associations 2026 1.0 null Drug-Induced Liver Injury CTD Gene-Disease Associations 1.0 1.86806 generalized abnormality of skin HPO Gene-Disease Associations 1.0 null sevoflurane_homo sapiens_gpl570_gds2772 GEO Signatures of Differentially Expressed Genes for Small Molecules 1.0 null Pulmonary Embolism DisGeNET Gene-Disease Associations 1.0 null PMC9319223__F2 PFOCR Pathway Figure Associations 2024 1.0 null leber optic atrophy HPO Gene-Disease Associations 1.0 null removes GeneRIF Biological Term Annotations 1.0 null abnormality of globe location HPO Gene-Disease Associations 1.0 null apnea HPO Gene-Disease Associations 1.0 null