YEM Search

搜索结果

LAMB2

靶点ID:TCMBANKGE012172

靶点别名:LAMS; NPHS5

靶点描述:laminin subunit beta 2

染色体:3

染色体位置:3p21.31

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6487

OMIM_Link:150325

Ensembl_Link:ENSG00000172037

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

TCMBANKIN059684	Vitamin E β-		C29H50O2	430.79	CC1=C(C(=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O
TCMBANKIN059746	α-tocopherol		C29H50O2	430.7 g/mol	CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C

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
TCMBANKDI000121	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI000576	-	Abnormality of the nervous system	Anatomical Abnormality	disease
TCMBANKDI001068	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI005226	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI006681	-	Abnormality of the immune system; Abnormality of the respiratory system	Disease or Syndrome	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007259	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007343	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI007350	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI007520	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI007707	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI010419	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI011210	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012363	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013453	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI014088	Respiratory Tract Diseases; Cardiovascular Diseases	Abnormality of the respiratory system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI018939	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI020337	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of limbs; Abnormality of the musculature	Finding	phenotype
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020574	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI020912	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI023021	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	group
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024199	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI025443	-	-	Disease or Syndrome	disease
TCMBANKDI025832	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI027248	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI030194	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI030938	-	-	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031591	Respiratory Tract Diseases	Abnormality of the respiratory system	Finding	phenotype
TCMBANKDI032521	-	Abnormality of the eye	Finding	phenotype