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HFM1

靶点ID:TCMBANKGE000355

靶点别名:MER3; POF9; SEC63D1; Si-11; Si-11-6; helicase

靶点描述:helicase for meiosis 1

染色体:1

染色体位置:1p22.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:20193

OMIM_Link:615684

Ensembl_Link:ENSG00000162669

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

TCMBANKIN036836	Vitisin B

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000023		Skin and Connective Tissue Diseases; Immune System Diseases	Abnormality of the immune system	Disease or Syndrome	disease
TCMBANKDI000432		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Congenital Abnormality	disease
TCMBANKDI000999		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI001180		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI003353		Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI008387		Pathological Conditions, Signs and Symptoms	Abnormality of the genitourinary system; Abnormality of the endocrine system	Finding	phenotype
TCMBANKDI011402		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI011983		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI018319		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms	-	Disease or Syndrome	disease
TCMBANKDI018680		Eye Diseases; Immune System Diseases; Endocrine System Diseases	Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI024839		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases	-	Disease or Syndrome	disease
TCMBANKDI024930		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases	-	Disease or Syndrome	disease