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AP3B1

靶点ID:TCMBANKGE009980

靶点别名:ADTB3; ADTB3A; HPS; HPS2; PE

靶点描述:adaptor related protein complex 3 subunit beta 1

染色体:5

染色体位置:5q14.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:566

OMIM_Link:603401

Ensembl_Link:ENSG00000132842

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

TCMBANKDI000092	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI001706	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI002245	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007501	-	Abnormality of the integument	Finding	phenotype
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI010160	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	group
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI015517	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020602	Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI020603	Pathological Conditions, Signs and Symptoms	-	Anatomical Abnormality	phenotype
TCMBANKDI022768	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI026625	Respiratory Tract Diseases	Abnormality of the respiratory system	Disease or Syndrome	group
TCMBANKDI028931	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI029220	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI031531	Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease
TCMBANKDI032321	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases	-	Disease or Syndrome	disease
TCMBANKDI032495	Hemic and Lymphatic Diseases	-	Disease or Syndrome	disease