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SRCAP

靶点ID:TCMBANKGE008249

靶点别名:DOMO1; EAF1; FLHS; SWR1

靶点描述:Snf2 related CREBBP activator protein

染色体:16

染色体位置:16p11.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:16974

OMIM_Link:611421

Ensembl_Link:ENSG00000080603

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

TCMBANKIN057906	mercury	hydrargyrum	Hg	200.59 g/mol	[Hg]
TCMBANKIN060958	oleic acid;cis-oleic acid;oleinic acid		C18H34O2	282.46	CCCCCCCCC=CCCCCCCCC(=O)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000974	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI001342	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI004910	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI006068	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI006401	-	Abnormality of the nervous system	Disease or Syndrome	phenotype
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012128	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI016026	Neoplasms; Eye Diseases	Neoplasm; Abnormality of the eye	Neoplastic Process	disease
TCMBANKDI016504	Pathological Conditions, Signs and Symptoms	Abnormality of the integument	Finding	phenotype
TCMBANKDI017675	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018145	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI018151	Digestive System Diseases; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI022188	-	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI023280	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024367	-	Abnormality of the integument	Anatomical Abnormality	phenotype
TCMBANKDI024381	Stomatognathic Diseases	Abnormality of head or neck	Anatomical Abnormality	disease
TCMBANKDI025171	Otorhinolaryngologic Diseases	Abnormality of the immune system; Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI026419	-	Abnormality of the voice	Finding	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI028831	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	-	Disease or Syndrome	disease
TCMBANKDI029054	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029520	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease