YEM Search

搜索结果

SIX6

靶点ID:TCMBANKGE004012

靶点别名:MCOPCT2; ODRMD; OPTX2; Six9

靶点描述:SIX homeobox 6

染色体:14

染色体位置:14q23.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:10892

OMIM_Link:606326

Ensembl_Link:ENSG00000184302

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

TCMBANKHE004828/YEM-712	Narcissus tazetta\|Narcissus tazetta L.var.chinensis Roem	水仙	多花水仙\|水仙		云南民族药物志：第四卷		阿昌族/傣族/德昂族/景颇族/傈僳族

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

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
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
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008314	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI011743	Neoplasms; Skin and Connective Tissue Diseases	Neoplasm; Abnormality of the breast	Neoplastic Process	group
TCMBANKDI011779	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI014056	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI014253	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI014941	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI015238	Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI016096	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI016840	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI020860	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Congenital Abnormality	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
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI025113	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI027961	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI029520	Mental Disorders	-	Mental or Behavioral Dysfunction	group
TCMBANKDI029922	Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI030301	Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI031189	Neoplasms	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031630	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype