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PHIP

靶点ID:TCMBANKGE011383

靶点别名:BRWD2; CHUJANS; DCAF14; DIDOD; WDR11; ndrp

靶点描述:pleckstrin homology domain interacting protein

染色体:6

染色体位置:6q14.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:15673

OMIM_Link:612870

Ensembl_Link:ENSG00000146247

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
TCMBANKDI000107	Behavior and Behavior Mechanisms	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI000485	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI008874	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010203	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI014088	Respiratory Tract Diseases; Cardiovascular Diseases	Abnormality of the respiratory system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI017008	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017183	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI017673	-	-	Clinical Attribute	phenotype
TCMBANKDI018016	Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI018290	Endocrine System Diseases	Abnormality of the genitourinary system; Abnormality of the endocrine system; Growth abnormality	Disease or Syndrome	disease
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI024987	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of head or neck; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI027324	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI028357	Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases	Abnormality of the immune system	Finding	phenotype
TCMBANKDI028775	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease