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靶点ID:TCMBANKGE010485

靶点别名:C14orf10; G4-1; G5pr; GDRM; SPGF36

靶点描述:protein phosphatase 2 regulatory subunit B''gamma

染色体:14

染色体位置:14q13.2

靶点类型:protein-coding

HERB_ID:HBTAR008123

HGNC_Link:17485

OMIM_Link:615902

Ensembl_Link:ENSG00000092020

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

TCMBANKDI002490		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI002512		Digestive System Diseases	Abnormality of the digestive system; Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI004489		-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI006629		-	-	Finding	phenotype
TCMBANKDI012319		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013728		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013972		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI015238		Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI017183		-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI022394		-	-	Laboratory Procedure	phenotype
TCMBANKDI027961		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI030467		-	Abnormality of the integument	Finding	phenotype
TCMBANKDI031134		-	Abnormality of the integument	Finding	phenotype
TCMBANKDI031417		Skin and Connective Tissue Diseases	Abnormality of the integument	Sign or Symptom	phenotype