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CLDN10

靶点ID:TCMBANKGE002359

靶点别名:CPETRL3; HELIX; OSP-L; OSPL

靶点描述:claudin 10

染色体:13

染色体位置:13q32.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:2033

OMIM_Link:617579

Ensembl_Link:ENSG00000134873

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

TCMBANKHE004828/YEM-712	Narcissus tazetta\|Narcissus tazetta L.var.chinensis Roem	水仙	多花水仙\|水仙		云南民族药物志：第四卷		阿昌族/傣族/德昂族/景颇族/傈僳族

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

TCMBANKDI003037		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Sign or Symptom	phenotype
TCMBANKDI003353		Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI007091		Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI012420		Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI018819		-	-	Laboratory Procedure	phenotype
TCMBANKDI019825		Neoplasms	-	Neoplastic Process	disease
TCMBANKDI023366		Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system	Disease or Syndrome	phenotype
TCMBANKDI029220		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Disease or Syndrome	disease
TCMBANKDI029861		Neoplasms; Hemic and Lymphatic Diseases	-	Neoplastic Process	disease
TCMBANKDI030540		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases	Abnormality of the genitourinary system; Neoplasm	Neoplastic Process	disease
TCMBANKDI030635		Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI031189		Neoplasms	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI031192		Neoplasms; Male Urogenital Diseases	-	Neoplastic Process	disease
TCMBANKDI031381		Neoplasms; Hemic and Lymphatic Diseases	-	Neoplastic Process	disease
TCMBANKDI031417		Skin and Connective Tissue Diseases	Abnormality of the integument	Sign or Symptom	phenotype