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PNPLA6

靶点ID:TCMBANKGE006661

靶点别名:BNHS; LNMS; NTE; NTEMND; OMCS; SPG39; iPLA2delta; sws

靶点描述:patatin like phospholipase domain containing 6

染色体:19

染色体位置:19p13.2

靶点类型:protein-coding

HERB_ID:HBTAR006087

HGNC_Link:16268

OMIM_Link:603197

Ensembl_Link:ENSG00000032444

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

TCMBANKIN026435	dithioerythritol		C4H10O2S2	154.3 g/mol	C(C(C(CO)S)S)O
TCMBANKIN057906	mercury	hydrargyrum	Hg	200.59 g/mol	[Hg]
TCMBANKIN057911	se	selenium	H2Se	78.97 g/mol	[Se]
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

TCMBANKDI000690	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI001673	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI002557	Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases	-	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
TCMBANKDI003627	Nervous System Diseases	Abnormality of the nervous 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
TCMBANKDI004344	Nervous System Diseases; Endocrine System Diseases	-	Disease or Syndrome	group
TCMBANKDI006349	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI007123	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007343	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI009080	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI010717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI011645	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011828	Chemically-Induced Disorders; Mental Disorders	-	Mental or Behavioral Dysfunction	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI014374	-	Abnormality of the endocrine system	Finding	phenotype
TCMBANKDI016439	Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI017308	Endocrine System Diseases	Abnormality of the endocrine system; Growth abnormality	Pathologic Function	phenotype
TCMBANKDI017469	Skin and Connective Tissue Diseases	Abnormality of the breast	Disease or Syndrome	disease
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018731	Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI019744	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI022182	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI023170	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI023464	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024145	Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI027322	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Disease or Syndrome	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI029728	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI029922	Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI030655	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI030993	Neoplasms; Nervous System Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease