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PIEZO2

靶点ID:TCMBANKGE011810

靶点别名:C18orf30; C18orf58; DA3; DA5; DAIPT; FAM38B; FAM38B2; HsT748; HsT771; MWKS

靶点描述:piezo type mechanosensitive ion channel component 2

染色体:18

染色体位置:18p11.22-p11.21

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:26270

OMIM_Link:613629

Ensembl_Link:ENSG00000154864

靶点对应的植物

ID	拉丁名	药名	药用植物名	功能与主治	来源	药用部位	使用民族

靶点对应的化合物

化合物ID	化合物名	别名	分子式	分子质量	Smiles

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000009	Neoplasms	Abnormality of the nervous system; Neoplasm	Neoplastic Process	disease
TCMBANKDI000066	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI000485	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI001033	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI001889	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004054	Pathological Conditions, Signs and Symptoms	-	Neoplastic Process	phenotype
TCMBANKDI004134	-	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI004280	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI007963	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI007994	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI008156	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI008377	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI008884	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	-	Disease or Syndrome	group
TCMBANKDI009275	Pathological Conditions, Signs and Symptoms	-	Sign or Symptom	phenotype
TCMBANKDI010413	-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011779	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI012128	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI012354	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013723	-	-	Finding	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI016031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016086	-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI016776	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI017762	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018930	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI019650	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020914	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI020958	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI022768	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI023185	Pathological Conditions, Signs and Symptoms	Abnormality of head or neck	Finding	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI025265	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI025502	-	-	Laboratory Procedure	phenotype
TCMBANKDI025832	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI027326	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Congenital Abnormality	group
TCMBANKDI027721	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI027961	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028111	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI029222	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI029461	Pathological Conditions, Signs and Symptoms	-	Sign or Symptom	phenotype
TCMBANKDI030221	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI030727	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI031083	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031221	-	Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype