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TRPM1

靶点ID:TCMBANKGE012213

靶点别名:CSNB1C; LTRPC1; MLSN1

靶点描述:transient receptor potential cation channel subfamily M member 1

染色体:15

染色体位置:15q13.3

靶点类型:protein-coding

HERB_ID:HBTAR002505

HGNC_Link:7146

OMIM_Link:603576

Ensembl_Link:ENSG00000134160

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

TCMBANKIN059724	Phenol, 2-methyl-5-(1-methylethyl)		C10H14O	150.22 g/mol	CC1=C(C=C(C=C1)C(C)C)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000054		Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI000590		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI003248		Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI005749		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI008884		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	-	Disease or Syndrome	group
TCMBANKDI011730		Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI015485		Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI016758		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI021278		Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI021886		-	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI028799		Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI031417		Skin and Connective Tissue Diseases	Abnormality of the integument	Sign or Symptom	phenotype