Showing entry for Tachykinin-3


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT021699
Protein NameTachykinin-3
Uniport IdQ9UHF0
GeneTAC3
Gene Id6866
DomainNeurokinin_B
Pfam PF03823  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
3. Environmental Information Processing 3.3 Signaling molecules and interaction hsa04080 Neuroactive ligand-receptor interaction
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0007565 female pregnancy
Biological Process GO:0007186 G protein-coupled receptor signaling pathway
Biological Process GO:0007218 neuropeptide signaling pathway
Biological Process GO:0045777 positive regulation of blood pressure
Biological Process GO:1902093 positive regulation of flagellated sperm motility
Biological Process GO:0007217 tachykinin receptor signaling pathway
molecular function GO:0031836 neuromedin K receptor binding
molecular function GO:0005102 signaling receptor binding
molecular function GO:0031837 substance K receptor binding
cellular component GO:0005576 extracellular region
cellular component GO:0005615 extracellular space
Reactome
Pathway Id Pathway Name
R-HSA-162582 Signal Transduction
R-HSA-372790 Signaling by GPCR
R-HSA-373076 Class A/1 (Rhodopsin-like receptors)
R-HSA-375276 Peptide ligand-binding receptors
R-HSA-380095 Tachykinin receptors bind tachykinins
R-HSA-388396 GPCR downstream signalling
R-HSA-416476 G alpha (q) signalling events
R-HSA-500792 GPCR ligand binding
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0001857 BXGD000085 AIDS related complex Infections; Immune System Diseases
C0003467 BXGD000194 Anxiety Behavior and Behavior Mechanisms
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0008925 BXGD000575 Cleft Palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0010417 BXGD000670 Cryptorchidism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
C0011581 BXGD000733 Depressive disorder Mental Disorders
C0011854 BXGD000753 Diabetes Mellitus, Insulin-Dependent Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0013537 BXGD000853 Eclampsia Female Urogenital Diseases and Pregnancy Complications
C0017601 BXGD001125 Glaucoma Eye Diseases
C0018418 BXGD001192 Gynecomastia Skin and Connective Tissue Diseases
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020619 BXGD001447 Hypogonadism Endocrine System Diseases
C0022735 BXGD001581 Klinefelter Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0022876 BXGD001591 Premature Obstetric Labor Female Urogenital Diseases and Pregnancy Complications
C0023267 BXGD001626 Fibroid Tumor Neoplasms
C0026769 BXGD001930 Multiple Sclerosis Immune System Diseases; Nervous System Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029453 BXGD002154 Osteopenia Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029456 BXGD002157 Osteoporosis Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0032460 BXGD002355 Polycystic Ovary Syndrome Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0032914 BXGD002379 Pre-Eclampsia Female Urogenital Diseases and Pregnancy Complications
C0034012 BXGD002449 Delayed Puberty Endocrine System Diseases
C0034013 BXGD002450 Precocious Puberty Endocrine System Diseases
C0042133 BXGD002960 Uterine Fibroids Neoplasms
C0151721 BXGD003465 Testicular hypogonadism Endocrine System Diseases
C0152459 BXGD003600 Linear atrophy Pathological Conditions, Signs and Symptoms
C0220748 BXGD004336 Cartilage-hair hypoplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Immune System Diseases
C0221369 BXGD004453 Acquired Camptodactyly
C0232939 BXGD004568 Primary physiologic amenorrhea Pathological Conditions, Signs and Symptoms
C0232940 BXGD004569 Secondary physiologic amenorrhea Pathological Conditions, Signs and Symptoms
C0233514 BXGD004584 Abnormal behavior Behavior and Behavior Mechanisms
C0241355 BXGD005092 Small testicle
C0242350 BXGD005154 Erectile dysfunction Male Urogenital Diseases; Mental Disorders
C0262444 BXGD005244 Abnormality of the dentition Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0266013 BXGD005606 Congenital hypoplasia of breast Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0266399 BXGD005663 Infantile uterus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0271578 BXGD006216 Female hypogonadism syndrome Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases; Endocrine System Diseases
C0271623 BXGD006222 Hypogonadotropic hypogonadism Endocrine System Diseases
C0276289 BXGD006418 Zika Virus Infection Infections
C0341862 BXGD007426 Hypothalamic amenorrhea Nervous System Diseases; Endocrine System Diseases
C0342384 BXGD007470 Idiopathic hypogonadotropic hypogonadism Endocrine System Diseases
C0342544 BXGD007501 Idiopathic central precocious puberty Endocrine System Diseases
C0425957 BXGD008555 Secondary amenorrhea Pathological Conditions, Signs and Symptoms
C0427460 BXGD008616 Red cell distribution width determination
C0541764 BXGD009259 Delayed bone age
C0600142 BXGD009696 Hot flushes Pathological Conditions, Signs and Symptoms
C0685409 BXGD009810 Congenital Camptodactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0685840 BXGD009821 Congenital hypoplasia of ovary Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0848259 BXGD010878 male puberty
C0948896 BXGD011563 Primary hypogonadism Endocrine System Diseases
C1304746 BXGD012343 RDW - Red blood cell distribution width result
C1387005 BXGD012953 Penis agenesis Male Urogenital Diseases
C1611743 BXGD013456 Familial (FPAH)
C1827524 BXGD013773 Wide spaced nipples
C1836308 BXGD014107 Generalized joint laxity
C1836542 BXGD014129 Depressed nasal bridge
C1846228 BXGD014793 Absence of pubertal development
C1862863 BXGD016138 Sparse body hair
C1865866 BXGD016345 Congenital sensorineural hearing loss Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C2113596 BXGD016924 Idiopathic Precocious Puberty Endocrine System Diseases
C2931689 BXGD018049 Dystrophia myotonica 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C3250443 BXGD018584 MYOTONIC DYSTROPHY 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C3489396 BXGD018929 Hypogonadism, Isolated Hypogonadotropic Endocrine System Diseases
C3553843 BXGD019193 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA
C3899503 BXGD020084 Congenital hypogonadotropic hypogonadism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
C4016274 BXGD020299 HYPOGONADOTROPIC HYPOGONADISM 10 WITHOUT ANOSMIA
C4021107 BXGD020557 Non-obstructive azoospermia Male Urogenital Diseases
C4021551 BXGD020667 Absence of secondary sex characteristics
C4021776 BXGD020772 Abnormality of the voice
C4022675 BXGD020952 Increased female libido
C4025569 BXGD021668 Eunuchoid habitus Pathological Conditions, Signs and Symptoms
C4025901 BXGD021856 Abnormality of body height
C4073137 BXGD022045 Decreased serum testosterone level
C4552011 BXGD023477 Gonadotropin deficiency
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002616 Copper 63.55
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein