YEM Search

搜索结果

KCNK4

靶点ID:TCMBANKGE001554

靶点别名:FHEIG; K2p4.1; TRAAK; TRAAK1

靶点描述:potassium two pore domain channel subfamily K member 4

染色体:11

染色体位置:11q13.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:6279

OMIM_Link:605720

Ensembl_Link:ENSG00000182450

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

TCMBANKIN057960	glutathion	glutathione	C10H17N3O6S	307.33 g/mol	C(CC(=O)NC(CS)C(=O)NCC(=O)O)C(C(=O)O)N
TCMBANKIN061221	n-propanol		C3H8O	60.1 g/mol	CCCO

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000763		-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI001342		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI002718		-	-	Finding	phenotype
TCMBANKDI004489		-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI006165		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007228		-	-	Finding	phenotype
TCMBANKDI013008		Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI013728		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI017965		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020119		Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI024934		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI028305		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease