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GRIP1

靶点ID:TCMBANKGE010953

靶点别名:FRASRS3; GRIP

靶点描述:glutamate receptor interacting protein 1

染色体:12

染色体位置:12q14.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:18708

OMIM_Link:604597

Ensembl_Link:ENSG00000155974

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

TCMBANKIN058460	pedatisectine b		C5H5N5	135.13 g/mol	C1=NC2=NC=NC(=C2N1)N

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI003536	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities	Abnormality of the digestive system; Abnormality of connective tissue	Congenital Abnormality	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	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
TCMBANKDI007043	Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007110	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI007539	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI009081	-	Abnormality of the eye	Anatomical Abnormality	phenotype
TCMBANKDI012460	-	Abnormality of head or neck	Anatomical Abnormality	disease
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI015186	-	Abnormality of the nervous system	Anatomical Abnormality	phenotype
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017896	Behavior and Behavior Mechanisms	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI019358	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI019697	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI020678	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Musculoskeletal Diseases; Male Urogenital Diseases	-	Disease or Syndrome	disease
TCMBANKDI022457	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI023602	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Abnormality of the digestive system	Finding	phenotype
TCMBANKDI023786	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI024381	Stomatognathic Diseases	Abnormality of head or neck	Anatomical Abnormality	disease
TCMBANKDI025220	-	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI029064	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease