Finterly

Hereditary leiomyomatosis and renal cell carcinoma pathway

Chemokine signaling

Primary focal segmental glomerulosclerosis (FSGS)

Fragile X syndrome

GABA receptor signaling

Ferroptosis

Small cell lung cancer

Cerebral organic acidurias, including diseases

Non-small cell lung cancer

Mammary gland development: pregnancy and lactation - stage 3 of 4

Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism

Purine metabolism

Ketogenesis and ketolysis

Alternative pathway of fetal androgen synthesis

Molybdenum cofactor (Moco) biosynthesis

Cysteine and methionine catabolism

Methionine metabolism leading to sulfur amino acids and related disorders

Degradation pathway of sphingolipids, including diseases

Methionine de novo and salvage pathway

Aerobic glycolysis - augmented

Mitochondrial complex I inhibition leading to parkinsonian motor deficits

HIF1A and PPARG in hypertrophic cardiomyopathy

Amyotrophic lateral sclerosis (ALS)

Cardiac progenitor differentiation

Glycogen synthesis and degradation

Metabolic pathway of LDL, HDL and TG, including diseases

Wnt signaling and pluripotency

Arrhythmogenic right ventricular cardiomyopathy

Pyrimidine metabolism

Liver steatosis adverse outcome pathway

Prader-Willi and Angelman syndrome

Prion disease pathway

Vitamin B12 disorders

Disorders of folate metabolism and transport

Krebs cycle disorders

GABA metabolism (aka GHB)

SREBF and miR33 in cholesterol and lipid homeostasis

EGF/EGFR signaling pathway

Toll-like receptor signaling

DNA damage response

Sudden infant death syndrome (SIDS) susceptibility pathways

Complement and coagulation cascades

Biogenic amine synthesis

Regulation of actin cytoskeleton

Pleural mesothelioma

Steroid biosynthesis

Purine metabolism and related disorders

miRNA regulation of DNA damage response

Wnt signaling pathway

Melanoma

Hepatitis B infection

Tryptophan metabolism

Measles virus infection

Modified nucleosides derived from tRNA as urinary cancer markers

Non-homologous end joining

EGF/EGFR signaling

Oxidation by cytochrome P450

Ras signaling

Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine

Bladder cancer

Nanomaterial induced apoptosis

Retinoblastoma gene in cancer

Homologous recombination

TCA cycle (aka Krebs or citric acid cycle)

DNA damage response (only ATM dependent)

ErbB signaling

Epithelial to mesenchymal transition in colorectal cancer

MET in type 1 papillary renal cell carcinoma

Vitamin D-sensitive calcium signaling in depression

Glycosylation and related congenital defects

Nucleotide excision repair

Genes controlling nephrogenesis

Acute viral myocarditis

Base excision repair

Mammalian disorder of sexual development

Type I interferon induction and signaling during SARS-CoV-2 infection

Male mating

T-cell activation SARS-CoV-2

Neuroinflammation and glutamatergic signaling

Endoplasmic reticulum stress response in coronavirus infection

Pathogenesis of SARS-CoV-2 mediated by nsp9-nsp10 complex

Major receptors targeted by epinephrine and norepinephrine

Metabolism of alpha-linolenic acid

Blood clotting and drug effects

Proximal tubule transport

ACE2 inhibition leads to pulmonary fibrosis

Genes associated with the development of rheumatoid arthritis

Kynurenine pathway and links to cell senescence

Hijack of ubiquitination by SARS-CoV-2

Influence of laminopathies on Wnt signaling

Mitochondrial immune response to SARS-CoV-2

Rett syndrome

Quercetin and Nf-kB / AP-1 induced apoptosis

Perturbations to host-cell autophagy, induced by SARS-CoV-2 proteins

Oligodendrocyte specification and differentiation, leading to myelin components for CNS

Mitochondrial complex I inhibition leading to chemical-induced Fanconi syndrome

Thiamine metabolic pathways

Intracellular auxin transport

Mitochondrial complex inhibition leading to liver injury

Host-pathogen interaction of human coronaviruses - interferon induction

Amino acid transport defects (IEMs)

Riboflavin and CoQ disorders

Vitamin B6-dependent and responsive disorders

Neurotransmitter disorders

Metabolism of sphingolipids in ER and Golgi apparatus

Ethylmalonic encephalopathy

Leucine, isoleucine and valine metabolism

Gamma-glutamyl cycle for the biosynthesis and degradation of glutathione, including diseases

Pyrimidine metabolism and related diseases

Proline and hydroxyproline pathways

Tyrosine metabolism and related disorders

Glycine metabolism, including IMDs

Fatty acid biosynthesis

Brassinolide biosynthetic pathway

Selenium micronutrient network

DNA IR-damage and cellular response via ATR

Salmonella virulence regulatory network

Serine metabolism

Trehalose degradation, low osmolarity

Nod-like receptor (NLR) signaling pathway

Biomarkers for pyrimidine metabolism disorders

Role of carnosine in muscle contraction

Hormonal control of pubertal growth spurt

Host-pathogen interaction of human coronaviruses - MAPK signaling

Biotin metabolism, including IMDs

Urea cycle and metabolism of amino groups

Distal convoluted tubule 1 (DCT1) cell

Cytokinin-auxin interactions in plant development

Cytokinin signaling

Polar auxin transport

Cannabinoid receptor signaling

Momilactone biosynthesis

MAPK signaling pathway

Estrogen signaling