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NOG

靶点ID:TCMBANKGE006856

靶点别名:SYM1; SYNS1; SYNS1A

靶点描述:noggin

染色体:17

染色体位置:17q22

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:7866

OMIM_Link:602991

Ensembl_Link:ENSG00000183691

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
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI000061	Digestive System Diseases; Neoplasms	Abnormality of the digestive system; Neoplasm	Neoplastic Process	group
TCMBANKDI000403	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI001706	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI002456	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002684	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003032	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003261	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003547	-	Abnormality of limbs; Abnormality of the skeletal system	Acquired Abnormality	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI006055	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI007044	-	-	Disease or Syndrome	disease
TCMBANKDI007251	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI008377	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI009935	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI011411	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012416	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI012932	Infections; Immune System Diseases	-	Disease or Syndrome	group
TCMBANKDI013541	Cardiovascular Diseases	-	Disease or Syndrome	group
TCMBANKDI014531	Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases	-	Neoplastic Process	disease
TCMBANKDI015224	Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases	Abnormality of the digestive system; Abnormality of the respiratory system	Anatomical Abnormality	disease
TCMBANKDI015238	Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI016504	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Finding	phenotype
TCMBANKDI016890	Digestive System Diseases; Neoplasms	-	Neoplastic Process	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017455	Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI017878	-	Abnormality of the ear	Finding	phenotype
TCMBANKDI018090	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI018890	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI019358	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI020860	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Congenital Abnormality	disease
TCMBANKDI021634	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI023185	Pathological Conditions, Signs and Symptoms	Abnormality of head or neck	Finding	phenotype
TCMBANKDI025854	Nutritional and Metabolic Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI027040	Immune System Diseases	-	Disease or Syndrome	disease
TCMBANKDI027337	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the ear	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028797	Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI030041	Hemic and Lymphatic Diseases	-	Neoplastic Process	disease
TCMBANKDI030653	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI031452	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease