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Eukaryotic proteases family

Root:   SCOP hierarchy in SUPERFAMILY [ 0] (11)
Class:   All beta proteins [ 48724] (174)
Fold:   Trypsin-like serine proteases [ 50493]
Superfamily:   Trypsin-like serine proteases [ 50494] (4)
Family:   Eukaryotic proteases [ 50514] (47)

DO

Disease Ontology (DO)

DO term FDR (all) SDDO (four levels) Annotation (direct or inherited)
Disease Ontology (DO)hereditary angioedema0.00002057--Direct
Disease Ontology (DO)angioedema0.001873--Inherited
Disease Ontology (DO)skin disease0.004207--Inherited
Disease Ontology (DO)pancreatic cancer0.01572--Inherited
Disease Ontology (DO)disease of anatomical entity0.01672--Inherited
Disease Ontology (DO)blood coagulation disease0.02422--Inherited
Disease Ontology (DO)pancreatic adenocarcinoma0.1485--Inherited
Disease Ontology (DO)cancer0.4738--Inherited
Disease Ontology (DO)disease of cellular proliferation0.5459--Inherited
Disease Ontology (DO)pancreatic carcinoma1--Inherited
Disease Ontology (DO)organ system cancer0.1848Least InformativeInherited
Disease Ontology (DO)hematopoietic system disease0.0000377Moderately InformativeDirect
Disease Ontology (DO)integumentary system disease0.02534Moderately InformativeInherited
Disease Ontology (DO)inherited blood coagulation disease0.0006963InformativeDirect
Disease Ontology (DO)endocrine gland cancer0.217InformativeInherited
Disease Ontology (DO)pancreatic ductal adenocarcinoma0.0009129Highly InformativeDirect

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HP

Human Phenotype (HP)

HP term FDR (all) SDHP (four levels) Annotation (direct or inherited)
Variable expressivity0--Direct
Phenotypic variability1--Inherited
Phenotypic Abnormality (PA)Abnormal prothrombin time0.000006834--Direct
Phenotypic Abnormality (PA)Decreased urine output0.00006267--Direct
Phenotypic Abnormality (PA)Microangiopathic hemolytic anemia0.000204--Direct
Phenotypic Abnormality (PA)Periodontitis0.0002766--Direct
Phenotypic Abnormality (PA)Premature loss of teeth0.000383--Direct
Phenotypic Abnormality (PA)Type I diabetes mellitus0.000383--Direct
Phenotypic Abnormality (PA)Abdominal pain0.0005915--Direct
Phenotypic Abnormality (PA)Abnormal circulating creatinine level0.0008697--Direct
Phenotypic Abnormality (PA)Prolonged partial thromboplastin time0.0009176--Direct
Phenotypic Abnormality (PA)Abnormality of humoral immunity0.005889--Inherited
Phenotypic Abnormality (PA)Abnormal oral mucosa morphology0.005915--Inherited
Phenotypic Abnormality (PA)Abnormality of blood circulation0.006317--Inherited
Phenotypic Abnormality (PA)Abnormality of renal excretion0.01903--Inherited
Phenotypic Abnormality (PA)Menstrual irregularities0.04502--Inherited
Phenotypic Abnormality (PA)Constitutional symptom0.06398--Inherited
Phenotypic Abnormality (PA)Abnormality of the kidney0.07754--Inherited
Phenotypic Abnormality (PA)Abnormal internal genitalia0.07807--Inherited
Phenotypic Abnormality (PA)Abnormal lung morphology0.0792--Inherited
Phenotypic Abnormality (PA)Abnormal circulating nitrogen compound concentration0.09359--Inherited
Phenotypic Abnormality (PA)Abnormality of prothrombin0.1222--Inherited
Phenotypic Abnormality (PA)Anemia due to reduced life span of red cells0.1319--Inherited
Phenotypic Abnormality (PA)Abnormality of the coagulation cascade0.1372--Inherited
Phenotypic Abnormality (PA)Abnormal bleeding0.1557--Inherited
Phenotypic Abnormality (PA)Abnormality of the female genitalia0.1557--Inherited
Phenotypic Abnormality (PA)Abnormal inflammatory response0.2307--Inherited
Phenotypic Abnormality (PA)Glucose intolerance0.3027--Inherited
Phenotypic Abnormality (PA)Abnormality of the respiratory system0.3116--Inherited
Phenotypic Abnormality (PA)Abnormality of female internal genitalia0.393--Inherited
Phenotypic Abnormality (PA)Abnormality of the urinary system0.5047--Inherited
Phenotypic Abnormality (PA)Abnormality of the genital system0.7163--Inherited
Phenotypic Abnormality (PA)Abnormality of the skeletal system0.718--Inherited
Phenotypic Abnormality (PA)Puberty and gonadal disorders0.8082--Inherited
Phenotypic Abnormality (PA)Abnormal oral morphology0.9032--Inherited
Phenotypic Abnormality (PA)Abnormality of head or neck0.9254--Inherited
Phenotypic Abnormality (PA)Abnormality of the mouth0.9505--Inherited
Phenotypic Abnormality (PA)Abnormality of the head0.964--Inherited
Phenotypic Abnormality (PA)Abdominal symptom0.993--Inherited
Phenotypic Abnormality (PA)Abnormal erythrocyte morphology1--Inherited
Phenotypic Abnormality (PA)Increased inflammatory response1--Inherited
Phenotypic Abnormality (PA)Abnormality of the digestive system0.1078Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the immune system0.1863Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the cardiovascular system0.2504Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of metabolism/homeostasis0.5126Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the genitourinary system0.6459Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the face0.8637Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the musculature1Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of skeletal morphology1Least InformativeInherited
Phenotypic Abnormality (PA)Abnormality of blood and blood-forming tissues0.000001139Moderately InformativeDirect
Phenotypic Abnormality (PA)Abnormality of immune system physiology0.07152Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal cardiovascular system physiology0.08874Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the upper urinary tract0.09174Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the urinary system physiology0.1072Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal circulating metabolite concentration0.1786Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal respiratory system morphology0.1944Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the endocrine system0.21Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal joint morphology0.3199Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of digestive system physiology0.3479Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal reproductive system morphology0.5815Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal homeostasis0.6383Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal skeletal muscle morphology0.9981Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormal oral cavity morphology1Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of coagulation0.0001582InformativeDirect
Phenotypic Abnormality (PA)Abnormality of complement system0.0001861InformativeDirect
Phenotypic Abnormality (PA)Abnormality of the gingiva0.000595InformativeDirect
Phenotypic Abnormality (PA)Abnormal renal physiology0.006594InformativeInherited
Phenotypic Abnormality (PA)Pain0.03867InformativeInherited
Phenotypic Abnormality (PA)Azotemia0.04833InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the menstrual cycle0.1078InformativeInherited
Phenotypic Abnormality (PA)Internal hemorrhage0.2109InformativeInherited
Phenotypic Abnormality (PA)Anemia0.2422InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the dentition0.5686InformativeInherited
Phenotypic Abnormality (PA)Abnormal glucose homeostasis0.5793InformativeInherited
Phenotypic Abnormality (PA)Abnormality of the nose0.6317InformativeInherited
Phenotypic Abnormality (PA)Joint hemorrhage0.000000001819Highly InformativeDirect
Phenotypic Abnormality (PA)Prolonged prothrombin time0.000005448Highly InformativeDirect
Phenotypic Abnormality (PA)Autoimmunity0.00001061Highly InformativeDirect
Phenotypic Abnormality (PA)Intramuscular hematoma0.00001237Highly InformativeDirect
Phenotypic Abnormality (PA)Epistaxis0.0001194Highly InformativeDirect
Phenotypic Abnormality (PA)Menorrhagia0.0002805Highly InformativeDirect
Phenotypic Abnormality (PA)Abnormality of the pleura0.000617Highly InformativeDirect
Phenotypic Abnormality (PA)Elevated serum creatinine0.0006188Highly InformativeDirect
Phenotypic Abnormality (PA)Abnormal urine output0.0008575Highly InformativeDirect
Phenotypic Abnormality (PA)Diabetes mellitus0.4551Highly InformativeInherited
Phenotypic Abnormality (PA)Hemolytic anemia1Highly InformativeInherited

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MP

Mouse Phenotype (MP)

MP term FDR (all) SDMP (four levels) Annotation (direct or inherited)
Mammalian Phenotype (MP)abnormal hemostasis0.00001714--Direct
Mammalian Phenotype (MP)decreased susceptibility to induced choroidal neovascularization0.00006641--Direct
Mammalian Phenotype (MP)liver fibrosis0.0001003--Direct
Mammalian Phenotype (MP)abnormal complement pathway0.0003347--Direct
Mammalian Phenotype (MP)abnormal trachea morphology0.0003419--Direct
Mammalian Phenotype (MP)choroidal neovascularization0.0004123--Direct
Mammalian Phenotype (MP)abnormal optic choroid morphology0.0006261--Direct
Mammalian Phenotype (MP)abnormal choroid vasculature morphology0.0007906--Direct
Mammalian Phenotype (MP)abnormal response to infection0.02313--Inherited
Mammalian Phenotype (MP)abnormal uvea morphology0.03508--Inherited
Mammalian Phenotype (MP)pathological neovascularization0.03639--Inherited
Mammalian Phenotype (MP)abnormal immune system physiology0.09763--Inherited
Mammalian Phenotype (MP)abnormal liver morphology0.3154--Inherited
Mammalian Phenotype (MP)abnormal cardiovascular system morphology0.4347--Inherited
Mammalian Phenotype (MP)abnormal hepatobiliary system morphology0.4646--Inherited
Mammalian Phenotype (MP)homeostasis/metabolism phenotype0.6059--Inherited
Mammalian Phenotype (MP)abnormal respiratory system morphology0.6107--Inherited
Mammalian Phenotype (MP)abnormal blood homeostasis0.688--Inherited
Mammalian Phenotype (MP)abnormal humoral immune response0.9168--Inherited
Mammalian Phenotype (MP)vision/eye phenotype0.9917--Inherited
Mammalian Phenotype (MP)immune system phenotype0.03043Least InformativeInherited
Mammalian Phenotype (MP)cardiovascular system phenotype0.5366Least InformativeInherited
Mammalian Phenotype (MP)abnormal homeostasis0.9667Least InformativeInherited
Mammalian Phenotype (MP)altered susceptibility to infection0.0006595Moderately InformativeDirect
Mammalian Phenotype (MP)abnormal cardiovascular system physiology0.2975Moderately InformativeInherited
Mammalian Phenotype (MP)liver/biliary system phenotype0.401Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal blood vessel morphology0.4183Moderately InformativeInherited
Mammalian Phenotype (MP)respiratory system phenotype0.788Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal eye morphology0.9984Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal blood coagulation0.00001571InformativeDirect
Mammalian Phenotype (MP)abnormal innate immunity0.01374InformativeInherited
Mammalian Phenotype (MP)abnormal blood vessel physiology0.4735InformativeInherited

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WP

Worm Phenotype (WP)

WP term FDR (all) SDWP (four levels) Annotation (direct or inherited)
Worm Phenotype (WP)basement membrane remodeling variant0.000005517--Direct
Worm Phenotype (WP)development variant1--Inherited
Worm Phenotype (WP)physiology variant1--Inherited
Worm Phenotype (WP)pericellular component development variant0.00001756Moderately InformativeDirect

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ZA

Zebrafish Anatomy (ZA)

ZA term FDR (all) SDZA (four levels) Annotation (direct or inherited)
Zebrafish Anatomy (ZA)whole organism0--Direct
Zebrafish Anatomy (ZA)anatomical system0--Direct
Zebrafish Anatomy (ZA)anatomical group0--Direct
Zebrafish Anatomy (ZA)anatomical structure1--Inherited

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XA

Xenopus Anatomy (XA)

XA term FDR (all) SDXA (four levels) Annotation (direct or inherited)
Xenopus ANatomical entity (XAN)anatomical structure0--Direct
Xenopus ANatomical entity (XAN)trunk region0.3632--Inherited
Xenopus ANatomical entity (XAN)compound organ0.9471--Inherited
Xenopus ANatomical entity (XAN)organism subdivision0.9654--Inherited
Xenopus ANatomical entity (XAN)anatomical region0.9978--Inherited
Xenopus ANatomical entity (XAN)anatomical group1--Inherited
Xenopus ANatomical entity (XAN)anatomical system1--Inherited
Xenopus ANatomical entity (XAN)whole organism1--Inherited
Xenopus ANatomical entity (XAN)multicellular anatomical structure1--Inherited
Xenopus ANatomical entity (XAN)anatomical cluster0.107Least InformativeInherited
Xenopus ANatomical entity (XAN)trunk0.3601Least InformativeInherited
Xenopus ANatomical entity (XAN)viscus0.04088Moderately InformativeInherited
Xenopus ANatomical entity (XAN)alimentary system0.05137Moderately InformativeInherited
Xenopus ANatomical entity (XAN)pancreas0.00002993Highly InformativeDirect

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EC

Enzyme Commission (EC)

EC term FDR (all) SDEC (four levels) Annotation (direct or inherited)
Enzyme Commission (EC)Trypsin0--Direct
Enzyme Commission (EC)Tissue kallikrein0.0000000000002123--Direct
Enzyme Commission (EC)Coagulation factor Xa0.0000000007636--Direct
Enzyme Commission (EC)Chymotrypsin0.000000004636--Direct
Enzyme Commission (EC)Plasmin0.0000009771--Direct
Enzyme Commission (EC)Coagulation factor IXa0.000001016--Direct
Enzyme Commission (EC)Protein C (activated)0.000002491--Direct
Enzyme Commission (EC)Tryptase0.000006097--Direct
Enzyme Commission (EC)T-plasminogen activator0.000006097--Direct
Enzyme Commission (EC)Pancreatic elastase0.00001492--Direct
Enzyme Commission (EC)Chymase0.00001492--Direct
Enzyme Commission (EC)U-plasminogen activator0.00001492--Direct
Enzyme Commission (EC)Acrosin0.00003659--Direct
Enzyme Commission (EC)Venombin A0.00003659--Direct
Enzyme Commission (EC)Coagulation factor VIIa0.00009001--Direct
Enzyme Commission (EC)Coagulation factor XIIa0.0002217--Direct
Enzyme Commission (EC)Complement subcomponent C1r0.0002217--Direct
Enzyme Commission (EC)Complement subcomponent C1s0.0002217--Direct
Enzyme Commission (EC)Classical-complement-pathway C3/C5 convertase0.0002217--Direct
Enzyme Commission (EC)Thrombin0.0002217--Direct
Enzyme Commission (EC)Pancreatic elastase II0.0002217--Direct
Enzyme Commission (EC)Complement factor D0.0005457--Direct
Enzyme Commission (EC)Alternative-complement-pathway C3/C5 convertase0.0005474--Direct
Enzyme Commission (EC)Hydrolases0Least InformativeDirect
Enzyme Commission (EC)Acting on peptide bonds (peptidases)0Moderately InformativeDirect
Enzyme Commission (EC)Serine endopeptidases0InformativeDirect

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CD

CTD Diseases (CD)

CD term FDR (all) SDCD (four levels) Annotation (direct or inherited)
CTD Diseases (CD)Hematologic Diseases0.000000002804--Direct
CTD Diseases (CD)Embolism and Thrombosis0.0000001131--Direct
CTD Diseases (CD)Bacterial Infections0.0001863--Direct
CTD Diseases (CD)Pulmonary Embolism0.0002484--Direct
CTD Diseases (CD)Cardiovascular Diseases0.0009397--Direct
CTD Diseases (CD)Blood Coagulation Disorders0.001187--Inherited
CTD Diseases (CD)Bacterial Infections and Mycoses0.001265--Inherited
CTD Diseases (CD)Primary Immunodeficiency Diseases0.00128--Inherited
CTD Diseases (CD)Immunologic Deficiency Syndromes0.005332--Inherited
CTD Diseases (CD)Thromboembolism0.01277--Inherited
CTD Diseases (CD)Congenital, Hereditary, and Neonatal Diseases and Abnormalities0.0676--Inherited
CTD Diseases (CD)Lung Diseases0.2187--Inherited
CTD Diseases (CD)Embolism0.3089--Inherited
CTD Diseases (CD)Pathologic Processes0.3493--Inherited
CTD Diseases (CD)Central Nervous System Diseases0.7572--Inherited
CTD Diseases (CD)Genetic Diseases, Inborn0.2369Least InformativeInherited
CTD Diseases (CD)Pathological Conditions, Signs and Symptoms0.813Least InformativeInherited
CTD Diseases (CD)Nervous System Diseases0.9619Least InformativeInherited
CTD Diseases (CD)Hemic and Lymphatic Diseases0.000006201Moderately InformativeDirect
CTD Diseases (CD)Vascular Diseases0.004496Moderately InformativeInherited
CTD Diseases (CD)Infections0.0485Moderately InformativeInherited
CTD Diseases (CD)Immune System Diseases0.1863Moderately InformativeInherited
CTD Diseases (CD)Respiratory Tract Diseases0.3491Moderately InformativeInherited
CTD Diseases (CD)Brain Diseases0.703Moderately InformativeInherited
CTD Diseases (CD)Blood Coagulation Disorders, Inherited0.0000000193InformativeDirect
CTD Diseases (CD)Hereditary Complement Deficiency Diseases0.000000343InformativeDirect
CTD Diseases (CD)Hemorrhage0.0009259InformativeDirect
CTD Diseases (CD)Cerebrovascular Disorders0.06243InformativeInherited
CTD Diseases (CD)Thrombophilia0.0005082Highly InformativeDirect
CTD Diseases (CD)Intracranial Embolism and Thrombosis0.0005936Highly InformativeDirect

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CC

CTD Chemicals (CC)

CC term FDR (all) SDCC (four levels) Annotation (direct or inherited)
CTD Chemicals (CC)Reproductive Control Agents0.00000000564--Direct
CTD Chemicals (CC)merbarone0.0000002242--Direct
CTD Chemicals (CC)estradiol valerate-dienogest0.0000004692--Direct
CTD Chemicals (CC)estradiol, norethindrone drug combination0.0000006842--Direct
CTD Chemicals (CC)NuvaRing0.0000325--Direct
CTD Chemicals (CC)Calcium Chloride0.00003383--Direct
CTD Chemicals (CC)Warfarin0.00006731--Direct
CTD Chemicals (CC)Ziram0.0001294--Direct
CTD Chemicals (CC)Dutasteride0.0001612--Direct
CTD Chemicals (CC)Thiobarbiturates0.0001612--Direct
CTD Chemicals (CC)Dichlorvos0.0002807--Direct
CTD Chemicals (CC)ethinyl estradiol-desogestrel combination0.000313--Direct
CTD Chemicals (CC)Calcium Compounds0.0004487--Direct
CTD Chemicals (CC)Azasteroids0.0005582--Direct
CTD Chemicals (CC)Medroxyprogesterone Acetate0.00057--Direct
CTD Chemicals (CC)Medroxyprogesterone0.0006028--Direct
CTD Chemicals (CC)norgestimate0.000746--Direct
CTD Chemicals (CC)6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid0.0009018--Direct
CTD Chemicals (CC)Norpregnatrienes0.001261--Inherited
CTD Chemicals (CC)Estrogenic Steroids, Alkylated0.001261--Inherited
CTD Chemicals (CC)Hydroxyprogesterones0.002536--Inherited
CTD Chemicals (CC)Norpregnenes0.05489--Inherited
CTD Chemicals (CC)Pregnenediones0.07583--Inherited
CTD Chemicals (CC)Pregnenes0.08184--Inherited
CTD Chemicals (CC)Corpus Luteum Hormones0.1137--Inherited
CTD Chemicals (CC)Progesterone Congeners0.1208--Inherited
CTD Chemicals (CC)Estradiol0.6581--Inherited
CTD Chemicals (CC)Organic Chemicals0.6893--Inherited
CTD Chemicals (CC)Estradiol Congeners0.7169--Inherited
CTD Chemicals (CC)Gonadal Hormones0.7845--Inherited
CTD Chemicals (CC)Hormones, Hormone Substitutes, and Hormone Antagonists0.8374--Inherited
CTD Chemicals (CC)Physiological Effects of Drugs0.8454--Inherited
CTD Chemicals (CC)Hydrochloric Acid0.9446--Inherited
CTD Chemicals (CC)Carbamates0.9587--Inherited
CTD Chemicals (CC)Heterocyclic Compounds, Fused-Ring1--Inherited
CTD Chemicals (CC)Acids, Acyclic1--Inherited
CTD Chemicals (CC)Acids, Noncarboxylic1--Inherited
CTD Chemicals (CC)Anions1--Inherited
CTD Chemicals (CC)Carboxylic Acids1--Inherited
CTD Chemicals (CC)Estrenes1--Inherited
CTD Chemicals (CC)Heterocyclic Compounds1--Inherited
CTD Chemicals (CC)Heterocyclic Compounds, 1-Ring1--Inherited
CTD Chemicals (CC)Heterocyclic Compounds, 2-Ring1--Inherited
CTD Chemicals (CC)Hormones1--Inherited
CTD Chemicals (CC)Inorganic Chemicals1--Inherited
CTD Chemicals (CC)Ions1--Inherited
CTD Chemicals (CC)Norpregnanes1--Inherited
CTD Chemicals (CC)Polycyclic Compounds1--Inherited
CTD Chemicals (CC)Pyrans1--Inherited
CTD Chemicals (CC)Pyrimidinones1--Inherited
CTD Chemicals (CC)Steroids1--Inherited
CTD Chemicals (CC)Pharmacologic Actions1--Inherited
CTD Chemicals (CC)Fused-Ring Compounds1Least InformativeInherited
CTD Chemicals (CC)Acids1Least InformativeInherited
CTD Chemicals (CC)Benzopyrans1Least InformativeInherited
CTD Chemicals (CC)Electrolytes1Least InformativeInherited
CTD Chemicals (CC)Pyrimidines1Least InformativeInherited
CTD Chemicals (CC)Sulfur Compounds1Least InformativeInherited
CTD Chemicals (CC)Chemical Actions and Uses1Least InformativeInherited
CTD Chemicals (CC)Estranes0.7966Moderately InformativeInherited
CTD Chemicals (CC)Pregnanes0.8088Moderately InformativeInherited
CTD Chemicals (CC)Organophosphorus Compounds1Moderately InformativeInherited
CTD Chemicals (CC)Gonadal Steroid Hormones1Moderately InformativeInherited
CTD Chemicals (CC)Chlorine Compounds1Moderately InformativeInherited
CTD Chemicals (CC)Molecular Mechanisms of Pharmacological Action1Moderately InformativeInherited
CTD Chemicals (CC)Norsteroids0.01981InformativeInherited
CTD Chemicals (CC)Thiocarbamates0.02899InformativeInherited
CTD Chemicals (CC)Organophosphates0.3349InformativeInherited
CTD Chemicals (CC)Testosterone Congeners0.4037InformativeInherited
CTD Chemicals (CC)Therapeutic Uses0.6414InformativeInherited
CTD Chemicals (CC)Progesterone0.7221InformativeInherited
CTD Chemicals (CC)Chlorides0.939InformativeInherited
CTD Chemicals (CC)Chromans1InformativeInherited
CTD Chemicals (CC)Coumarins1InformativeInherited
CTD Chemicals (CC)Enzyme Inhibitors1InformativeInherited
CTD Chemicals (CC)Nandrolone0.000003693Highly InformativeDirect
CTD Chemicals (CC)Gestodene0.000004688Highly InformativeDirect
CTD Chemicals (CC)4-Hydroxycoumarins0.000361Highly InformativeDirect
CTD Chemicals (CC)Protease Inhibitors0.0004859Highly InformativeDirect
CTD Chemicals (CC)Norethindrone0.000517Highly InformativeDirect
CTD Chemicals (CC)Steroids, Heterocyclic0.002494Highly InformativeInherited
CTD Chemicals (CC)Desogestrel0.004919Highly InformativeInherited
CTD Chemicals (CC)Dimethyldithiocarbamate0.03764Highly InformativeInherited
CTD Chemicals (CC)Norgestrel0.4452Highly InformativeInherited
CTD Chemicals (CC)Barbiturates0.9942Highly InformativeInherited
CTD Chemicals (CC)Ethinyl Estradiol1Highly InformativeInherited

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Distribution on sTOL

Plot distribution on species Tree Of Life (sTOL) for this domain, i.e., present or absent across genomes/tips
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