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OCRL

靶点ID:TCMBANKGE007997

靶点别名:Dent-2; INPP5F; LOCR; NPHL2; OCRL-1; OCRL1

靶点描述:OCRL inositol polyphosphate-5-phosphatase

染色体:X

染色体位置:Xq26.1

靶点类型:protein-coding

HERB_ID:HBTAR002799

HGNC_Link:8108

OMIM_Link:300535

Ensembl_Link:ENSG00000122126

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

TCMBANKDI000066	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI000078	Neoplasms; Skin and Connective Tissue Diseases	Abnormality of the integument; Neoplasm	Neoplastic Process	group
TCMBANKDI000107	Behavior and Behavior Mechanisms	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI000246	-	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI002213	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI002459	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002974	Neoplasms	-	Neoplastic Process	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004210	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007618	Hemic and Lymphatic Diseases	Abnormality of blood and blood-forming tissues	Disease or Syndrome	phenotype
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009870	-	Abnormality of the voice	Finding	disease
TCMBANKDI011167	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011982	Nutritional and Metabolic Diseases; Musculoskeletal Diseases	Abnormality of the skeletal system	Disease or Syndrome	disease
TCMBANKDI012242	-	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013453	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Finding	phenotype
TCMBANKDI013839	Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI015695	-	Abnormality of metabolism/homeostasis	Finding	phenotype
TCMBANKDI017308	Endocrine System Diseases	Abnormality of the endocrine system; Growth abnormality	Pathologic Function	phenotype
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI018151	Digestive System Diseases; Nutritional and Metabolic Diseases	-	Disease or Syndrome	group
TCMBANKDI018250	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI018434	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI019240	-	Abnormality of limbs; Abnormality of the skeletal system	Pathologic Function	phenotype
TCMBANKDI020794	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	disease
TCMBANKDI020956	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	-	Disease or Syndrome	phenotype
TCMBANKDI021387	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis	Disease or Syndrome	phenotype
TCMBANKDI022485	-	-	Diagnostic Procedure	phenotype
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI025171	Otorhinolaryngologic Diseases	Abnormality of the immune system; Abnormality of the ear	Disease or Syndrome	disease
TCMBANKDI025291	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI029220	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032034	-	Abnormality of the eye	Congenital Abnormality	disease