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USH2A

靶点ID:TCMBANKGE009796

靶点别名:RP39; US2; USH2; dJ1111A8.1

靶点描述:usherin

染色体:1

染色体位置:1q41

靶点类型:protein-coding

HERB_ID:HBTAR004295

HGNC_Link:12601

OMIM_Link:608400

Ensembl_Link:ENSG00000042781

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

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000004	Pathological Conditions, Signs and Symptoms	Constitutional symptom	Sign or Symptom	phenotype
TCMBANKDI000236	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI002657	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic 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
TCMBANKDI004059	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI004835	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI005344	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008112	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI008156	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI009877	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI010242	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms	-	Disease or Syndrome	disease
TCMBANKDI012926	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI014624	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	group
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017527	-	Abnormality of limbs	Anatomical Abnormality	phenotype
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018053	Eye Diseases; Skin and Connective Tissue Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI022182	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI022361	Pathological Conditions, Signs and Symptoms; Eye Diseases	-	Sign or Symptom	phenotype
TCMBANKDI026106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI026922	Infections; Nervous System Diseases; Animal Diseases	-	Disease or Syndrome	disease
TCMBANKDI027099	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases	Abnormality of the ear	Finding	phenotype
TCMBANKDI027197	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI029546	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI031336	-	-	Disease or Syndrome	disease
TCMBANKDI032498	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease