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SPATA5

靶点ID:TCMBANKGE014445

靶点别名:AFG2; EHLMRS; SPAF

靶点描述:spermatogenesis associated 5

染色体:4

染色体位置:4q28.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:18119

OMIM_Link:613940

Ensembl_Link:ENSG00000145375

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

TCMBANKDI000485		Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI003556		-	-	Disease or Syndrome	disease
TCMBANKDI004558		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI005528		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI008874		-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009080		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument; Abnormality of head or neck	Disease or Syndrome	disease
TCMBANKDI013209		-	Abnormality of metabolism/homeostasis; Abnormal cellular phenotype	Finding	phenotype
TCMBANKDI013540		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI015485		Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI017183		-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI020452		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI025924		-	Abnormality of limbs; Abnormality of the skeletal system	Sign or Symptom	phenotype
TCMBANKDI028357		Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases	Abnormality of the immune system	Finding	phenotype
TCMBANKDI031438		Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI031570		-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032357		-	Abnormality of the digestive system	Finding	phenotype