dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Kringle modules family

Root:   SCOP hierarchy in SUPERFAMILY [ 0] (11)
Class:   Small proteins [ 56992] (90)
Fold:   Kringle-like [ 57439]
Superfamily:   Kringle-like [ 57440] (2)
Family:   Kringle modules [ 57441] (6)

DO

Disease Ontology (DO)

DO term FDR (all) SDDO (four levels) Annotation (direct or inherited)
Disease Ontology (DO)arteriosclerotic cardiovascular disease0.000001997--Direct
Disease Ontology (DO)myocardial infarction0.00001002--Direct
Disease Ontology (DO)cerebral degeneration0.00005036--Direct
Disease Ontology (DO)blood coagulation disease0.0002161--Direct
Disease Ontology (DO)vascular disease0.0005149--Direct
Disease Ontology (DO)central nervous system disease0.001056--Inherited
Disease Ontology (DO)pancreatic adenocarcinoma0.001746--Inherited
Disease Ontology (DO)cardiovascular system disease0.001861--Inherited
Disease Ontology (DO)arteriosclerosis0.002784--Inherited
Disease Ontology (DO)breast ductal carcinoma0.003698--Inherited
Disease Ontology (DO)pancreatic cancer0.005391--Inherited
Disease Ontology (DO)breast cancer0.069--Inherited
Disease Ontology (DO)thoracic cancer0.1564--Inherited
Disease Ontology (DO)disease of anatomical entity0.1742--Inherited
Disease Ontology (DO)cancer0.4064--Inherited
Disease Ontology (DO)disease of cellular proliferation0.4367--Inherited
Disease Ontology (DO)brain disease0.4522--Inherited
Disease Ontology (DO)pancreatic carcinoma1--Inherited
Disease Ontology (DO)nervous system disease0.0121Least InformativeInherited
Disease Ontology (DO)organ system cancer0.0902Least InformativeInherited
Disease Ontology (DO)artery disease0.0001827Moderately InformativeDirect
Disease Ontology (DO)hematopoietic system disease0.0118Moderately InformativeInherited
Disease Ontology (DO)atherosclerosis0.000001955InformativeDirect
Disease Ontology (DO)coronary artery disease0.02079InformativeInherited
Disease Ontology (DO)breast carcinoma0.03901InformativeInherited
Disease Ontology (DO)endocrine gland cancer0.05745InformativeInherited
Disease Ontology (DO)leukodystrophy0.00002088Highly InformativeDirect
Disease Ontology (DO)pancreatic ductal adenocarcinoma0.0003738Highly InformativeDirect
Disease Ontology (DO)invasive ductal carcinoma0.0008141Highly InformativeDirect

LINKTO: Domain2BO Download and Domain2BO Algorithm

HP

Human Phenotype (HP)

HP term FDR (all) SDHP (four levels) Annotation (direct or inherited)
Phenotypic Abnormality (PA)Venous thrombosis0.001251--Inherited
Phenotypic Abnormality (PA)Abnormal thrombosis0.02131--Inherited
Phenotypic Abnormality (PA)Abnormality of blood and blood-forming tissues0.02868Moderately InformativeInherited
Phenotypic Abnormality (PA)Abnormality of coagulation0.000823InformativeDirect
Phenotypic Abnormality (PA)Deep venous thrombosis0.000004176Highly InformativeDirect

LINKTO: Domain2BO Download and Domain2BO Algorithm

MP

Mouse Phenotype (MP)

MP term FDR (all) SDMP (four levels) Annotation (direct or inherited)
Mammalian Phenotype (MP)decreased susceptibility to induced choroidal neovascularization0.0000002191--Direct
Mammalian Phenotype (MP)choroidal neovascularization0.000001693--Direct
Mammalian Phenotype (MP)abnormal acute phase protein level0.000005981--Direct
Mammalian Phenotype (MP)rectal prolapse0.000009979--Direct
Mammalian Phenotype (MP)abnormal choroid vasculature morphology0.00002404--Direct
Mammalian Phenotype (MP)abnormal rectum morphology0.00003158--Direct
Mammalian Phenotype (MP)abnormal optic choroid morphology0.00003158--Direct
Mammalian Phenotype (MP)pathological neovascularization0.0003584--Direct
Mammalian Phenotype (MP)polydactyly0.0004613--Direct
Mammalian Phenotype (MP)respiratory distress0.0005538--Direct
Mammalian Phenotype (MP)abnormal hemostasis0.0007027--Direct
Mammalian Phenotype (MP)liver fibrosis0.0007431--Direct
Mammalian Phenotype (MP)abnormal uvea morphology0.00235--Inherited
Mammalian Phenotype (MP)digestive/alimentary phenotype0.003572--Inherited
Mammalian Phenotype (MP)abnormal digit morphology0.006936--Inherited
Mammalian Phenotype (MP)abnormal liver morphology0.01709--Inherited
Mammalian Phenotype (MP)abnormal cardiovascular system morphology0.02257--Inherited
Mammalian Phenotype (MP)abnormal hepatobiliary system morphology0.02348--Inherited
Mammalian Phenotype (MP)abnormal limb morphology0.02369--Inherited
Mammalian Phenotype (MP)skeleton phenotype0.02863--Inherited
Mammalian Phenotype (MP)abnormal immune system physiology0.1327--Inherited
Mammalian Phenotype (MP)vision/eye phenotype0.1672--Inherited
Mammalian Phenotype (MP)abnormal respiratory system physiology0.1839--Inherited
Mammalian Phenotype (MP)homeostasis/metabolism phenotype0.195--Inherited
Mammalian Phenotype (MP)abnormal respiration0.2425--Inherited
Mammalian Phenotype (MP)abnormal blood homeostasis0.2505--Inherited
Mammalian Phenotype (MP)abnormal skeleton morphology0.9709--Inherited
Mammalian Phenotype (MP)cardiovascular system phenotype0.07141Least InformativeInherited
Mammalian Phenotype (MP)immune system phenotype0.3659Least InformativeInherited
Mammalian Phenotype (MP)abnormal homeostasis0.9565Least InformativeInherited
Mammalian Phenotype (MP)respiratory system phenotype0.01771Moderately InformativeInherited
Mammalian Phenotype (MP)liver/biliary system phenotype0.03533Moderately InformativeInherited
Mammalian Phenotype (MP)limbs/digits/tail phenotype0.04908Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal protein level0.07219Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal eye morphology0.137Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal bone structure0.2254Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal blood vessel morphology0.3222Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal cardiovascular system physiology0.3772Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal immune serum protein physiology0.4514Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal digestive system morphology0.9003Moderately InformativeInherited
Mammalian Phenotype (MP)abnormal eyelid morphology0.0005751InformativeDirect
Mammalian Phenotype (MP)abnormal blood coagulation0.0006759InformativeDirect
Mammalian Phenotype (MP)abnormal respiratory function0.003763InformativeInherited
Mammalian Phenotype (MP)abnormal innate immunity0.03263InformativeInherited
Mammalian Phenotype (MP)abnormal blood vessel physiology0.06946InformativeInherited
Mammalian Phenotype (MP)abnormal intestine morphology0.1108InformativeInherited
Mammalian Phenotype (MP)abnormal autopod morphology0.1266InformativeInherited
Mammalian Phenotype (MP)abnormal bone volume0.0009441Highly InformativeDirect
Mammalian Phenotype (MP)abnormal breathing pattern0.001908Highly InformativeInherited
Mammalian Phenotype (MP)abnormal large intestine morphology0.002481Highly InformativeInherited

LINKTO: Domain2BO Download and Domain2BO Algorithm

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)neural plate0.05597--Inherited
Xenopus ANatomical entity (XAN)primary germ layer0.7159--Inherited
Xenopus ANatomical entity (XAN)multicellular anatomical structure0.787--Inherited
Xenopus ANatomical entity (XAN)whole organism1--Inherited
Xenopus ANatomical entity (XAN)embryo0.5605Least InformativeInherited
Xenopus ANatomical entity (XAN)tissue0.6664Least InformativeInherited
Xenopus ANatomical entity (XAN)ectoderm1Moderately InformativeInherited
Xenopus ANatomical entity (XAN)neuroectoderm0.1469InformativeInherited
Xenopus ANatomical entity (XAN)neural groove0.0001596Highly InformativeDirect

LINKTO: Domain2BO Download and Domain2BO Algorithm

EC

Enzyme Commission (EC)

EC term FDR (all) SDEC (four levels) Annotation (direct or inherited)
Enzyme Commission (EC)Plasmin0--Direct
Enzyme Commission (EC)T-plasminogen activator0.000000000000001283--Direct
Enzyme Commission (EC)U-plasminogen activator0.00000000000002706--Direct
Enzyme Commission (EC)Coagulation factor XIIa0.0000000002006--Direct
Enzyme Commission (EC)Thrombin0.0000000002006--Direct
Enzyme Commission (EC)Protein-tyrosine kinases0.0000000005556--Direct
Enzyme Commission (EC)Transferring phosphorus-containing groups0.7069--Inherited
Enzyme Commission (EC)Hydrolases0Least InformativeDirect
Enzyme Commission (EC)Transferases1Least InformativeInherited
Enzyme Commission (EC)Acting on peptide bonds (peptidases)0Moderately InformativeDirect
Enzyme Commission (EC)Serine endopeptidases0InformativeDirect
Enzyme Commission (EC)Receptor protein-tyrosine kinase0.00000000001543Highly InformativeDirect

LINKTO: Domain2BO Download and Domain2BO Algorithm

CD

CTD Diseases (CD)

CD term FDR (all) SDCD (four levels) Annotation (direct or inherited)
CTD Diseases (CD)Embolism and Thrombosis0.00000000008692--Direct
CTD Diseases (CD)Intracranial Thrombosis0.0000001605--Direct
CTD Diseases (CD)Stroke0.00004297--Direct
CTD Diseases (CD)Cerebral Arterial Diseases0.00005692--Direct
CTD Diseases (CD)Cerebral Infarction0.00006156--Direct
CTD Diseases (CD)Hematologic Diseases0.0003603--Direct
CTD Diseases (CD)Infarction0.001903--Inherited
CTD Diseases (CD)Cardiovascular Diseases0.004636--Inherited
CTD Diseases (CD)Ischemia0.007113--Inherited
CTD Diseases (CD)Intracranial Arterial Diseases0.01401--Inherited
CTD Diseases (CD)Brain Infarction0.0154--Inherited
CTD Diseases (CD)Blood Coagulation Disorders0.01865--Inherited
CTD Diseases (CD)Thromboembolism0.02132--Inherited
CTD Diseases (CD)Pathologic Processes0.11--Inherited
CTD Diseases (CD)Central Nervous System Diseases0.112--Inherited
CTD Diseases (CD)Congenital, Hereditary, and Neonatal Diseases and Abnormalities0.1327--Inherited
CTD Diseases (CD)Neurologic Manifestations0.1685--Inherited
CTD Diseases (CD)Brain Ischemia0.1715--Inherited
CTD Diseases (CD)Neoplasms0.197Least InformativeInherited
CTD Diseases (CD)Genetic Diseases, Inborn0.2584Least InformativeInherited
CTD Diseases (CD)Pathological Conditions, Signs and Symptoms0.3466Least InformativeInherited
CTD Diseases (CD)Nervous System Diseases0.3477Least InformativeInherited
CTD Diseases (CD)Hemic and Lymphatic Diseases0.003849Moderately InformativeInherited
CTD Diseases (CD)Brain Diseases0.06746Moderately InformativeInherited
CTD Diseases (CD)Vascular Diseases0.08074Moderately InformativeInherited
CTD Diseases (CD)Signs and Symptoms0.204Moderately InformativeInherited
CTD Diseases (CD)Blood Coagulation Disorders, Inherited0.00007305InformativeDirect
CTD Diseases (CD)Hemorrhage0.0009645InformativeDirect
CTD Diseases (CD)Cerebrovascular Disorders0.004859InformativeInherited
CTD Diseases (CD)Necrosis0.01097InformativeInherited
CTD Diseases (CD)Neoplastic Processes0.01503InformativeInherited
CTD Diseases (CD)Coagulation Protein Disorders0.000004819Highly InformativeDirect
CTD Diseases (CD)Infarction, Middle Cerebral Artery0.00002591Highly InformativeDirect
CTD Diseases (CD)Pain0.0002142Highly InformativeDirect
CTD Diseases (CD)Neoplasm Metastasis0.0005732Highly InformativeDirect
CTD Diseases (CD)Intracranial Embolism and Thrombosis0.0008396Highly InformativeDirect
CTD Diseases (CD)Thrombophilia0.0009946Highly InformativeDirect

LINKTO: Domain2BO Download and Domain2BO Algorithm

CC

CTD Chemicals (CC)

CC term FDR (all) SDCC (four levels) Annotation (direct or inherited)
CTD Chemicals (CC)Heterocyclic Compounds, Fused-Ring0--Direct
CTD Chemicals (CC)Carboxylic Acids0--Direct
CTD Chemicals (CC)Heterocyclic Compounds0--Direct
CTD Chemicals (CC)Heterocyclic Compounds, 1-Ring0--Direct
CTD Chemicals (CC)Heterocyclic Compounds, 2-Ring0--Direct
CTD Chemicals (CC)Inorganic Chemicals0--Direct
CTD Chemicals (CC)Organic Chemicals0--Direct
CTD Chemicals (CC)Polycyclic Compounds0--Direct
CTD Chemicals (CC)Pyrans0--Direct
CTD Chemicals (CC)Toxins, Biological0--Direct
CTD Chemicals (CC)ethinyl estradiol-desogestrel combination0.000000472--Direct
CTD Chemicals (CC)Medroxyprogesterone Acetate0.00001197--Direct
CTD Chemicals (CC)Medroxyprogesterone0.00001244--Direct
CTD Chemicals (CC)6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid0.00003273--Direct
CTD Chemicals (CC)Oxygen Compounds0.0005387--Direct
CTD Chemicals (CC)Estradiol0.0007211--Direct
CTD Chemicals (CC)Norpregnenes0.0007814--Direct
CTD Chemicals (CC)Gonadal Hormones0.001519--Inherited
CTD Chemicals (CC)Hormones, Hormone Substitutes, and Hormone Antagonists0.001892--Inherited
CTD Chemicals (CC)Pregnenediones0.002321--Inherited
CTD Chemicals (CC)Hydroxyprogesterones0.00262--Inherited
CTD Chemicals (CC)Polysaccharides0.003411--Inherited
CTD Chemicals (CC)Norpregnatrienes0.004115--Inherited
CTD Chemicals (CC)Pregnenes0.009249--Inherited
CTD Chemicals (CC)Pharmacologic Actions0.009672--Inherited
CTD Chemicals (CC)Estrogenic Steroids, Alkylated0.0433--Inherited
CTD Chemicals (CC)Corpus Luteum Hormones0.04972--Inherited
CTD Chemicals (CC)Progesterone Congeners0.05209--Inherited
CTD Chemicals (CC)Physiological Effects of Drugs0.05458--Inherited
CTD Chemicals (CC)Estradiol Congeners0.1474--Inherited
CTD Chemicals (CC)Estrenes1--Inherited
CTD Chemicals (CC)Hormones1--Inherited
CTD Chemicals (CC)Norpregnanes1--Inherited
CTD Chemicals (CC)Steroids1--Inherited
CTD Chemicals (CC)Benzopyrans0Least InformativeDirect
CTD Chemicals (CC)Biological Factors0Least InformativeDirect
CTD Chemicals (CC)Electrolytes0Least InformativeDirect
CTD Chemicals (CC)Chemical Actions and Uses0.01657Least InformativeInherited
CTD Chemicals (CC)Fused-Ring Compounds0.03031Least InformativeInherited
CTD Chemicals (CC)Carbohydrates0.3011Least InformativeInherited
CTD Chemicals (CC)Gases0.0002047Moderately InformativeDirect
CTD Chemicals (CC)Estranes0.05171Moderately InformativeInherited
CTD Chemicals (CC)Pregnanes0.4273Moderately InformativeInherited
CTD Chemicals (CC)Gonadal Steroid Hormones1Moderately InformativeInherited
CTD Chemicals (CC)Acids, Heterocyclic0.0005347InformativeDirect
CTD Chemicals (CC)Progesterone0.001524InformativeInherited
CTD Chemicals (CC)Quinazolines0.01573InformativeInherited
CTD Chemicals (CC)Norsteroids0.05285InformativeInherited
CTD Chemicals (CC)Chromans0.1929InformativeInherited
CTD Chemicals (CC)Gestodene0.0000003506Highly InformativeDirect
CTD Chemicals (CC)Desogestrel0.000003682Highly InformativeDirect
CTD Chemicals (CC)Quinazolinones0.00003947Highly InformativeDirect
CTD Chemicals (CC)Norgestrel0.0004042Highly InformativeDirect
CTD Chemicals (CC)Glycosaminoglycans0.0009919Highly InformativeDirect
CTD Chemicals (CC)Ethinyl Estradiol1Highly InformativeInherited

LINKTO: Domain2BO Download and Domain2BO Algorithm

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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