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SIL1

靶点ID:TCMBANKGE012042

靶点别名:BAP; MSS; ULG5

靶点描述:SIL1 nucleotide exchange factor

染色体:5

染色体位置:5q31.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:24624

OMIM_Link:608005

Ensembl_Link:ENSG00000120725

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

TCMBANKDI000009	Neoplasms	Abnormality of the nervous system; Neoplasm	Neoplastic Process	disease
TCMBANKDI000054	Nervous System Diseases; Mental Disorders	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI000974	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI002475	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003184	Hemic and Lymphatic Diseases	Abnormality of the immune system; Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI003547	-	Abnormality of limbs; Abnormality of the skeletal system	Acquired Abnormality	disease
TCMBANKDI004857	Nervous System Diseases	-	Disease or Syndrome	group
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI007197	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007343	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI007444	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI010896	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	group
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011743	Neoplasms; Skin and Connective Tissue Diseases	Neoplasm; Abnormality of the breast	Neoplastic Process	group
TCMBANKDI012859	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI013913	Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018020	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI019748	Musculoskeletal Diseases	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI020306	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI030433	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031644	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease