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   CTNS

靶点ID:TCMBANKGE003422


靶点别名:CTNS-LSB; PQLC4; SLC66A4


靶点描述:cystinosin, lysosomal cystine transporter


染色体:17


染色体位置:17p13.2


靶点类型:protein-coding


HERB_ID:HBTAR000919


HGNC_Link:2518


OMIM_Link:606272


Ensembl_Link:ENSG00000040531


   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
TCMBANKIN057930 D-Cystine L-Dicysteine; CHEBI:16283; Cystine,d; C7602_SIGMA; Cystine D-form; C8755_SIGMA; Cystine, D-; 2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid; Cystine (USAN); 56-89-3; (R,R)-3,3'-dithiobis(2-aminopropanoic acid); 3,3'-Dithiobis-L-alanine; Gelucystine; 349-46-2; L-Cystine (9CI); bis(beta-amino-beta-carboxyethyl) disulfide; L-alpha-Diamino-beta-dithiolactic acid; C5735_SIGMA; (2R)-2-amino-3-[(2R)-2-amino-3-hydroxy-3-oxopropyl]disulfanylpropanoic acid; D03636; EINECS 206-486-2; (2R)-2-amino-3-[(2R)-2-amino-3-hydroxy-3-oxo-propyl]disulfanyl-propanoic acid; 30199_FLUKA; Cystine, L- (8CI); (2R,2'R)-3,3'-disulfanediylbis(2-aminopropanoic acid); NCGC00166006-01; (R,R)-3,3'-Dithiobis(2-aminopropionicacid); C00491; (2R)-2-amino-3-[(2R)-2-amino-3-hydroxy-3-keto-propyl]disulfanyl-propionic acid;cystine C6H12N2O4S2 240.3 C(C(C(=O)O)N)SSCC(C(=O)O)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
TCMBANKDI002213 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system Disease or Syndrome disease
TCMBANKDI003037 Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Abnormality of the genitourinary system Sign or Symptom phenotype
TCMBANKDI004210 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases - Disease or Syndrome disease
TCMBANKDI007520 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Abnormality of the genitourinary system Disease or Syndrome disease
TCMBANKDI009951 Nutritional and Metabolic Diseases; Musculoskeletal Diseases Abnormality of the skeletal system Disease or Syndrome disease
TCMBANKDI010066 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases - Disease or Syndrome; Congenital Abnormality disease
TCMBANKDI011209 Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system Finding phenotype
TCMBANKDI011982 Nutritional and Metabolic Diseases; Musculoskeletal Diseases Abnormality of the skeletal system Disease or Syndrome disease
TCMBANKDI012420 Skin and Connective Tissue Diseases Abnormality of the integument Disease or Syndrome disease
TCMBANKDI013453 Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Abnormality of metabolism/homeostasis; Abnormality of the genitourinary system Finding phenotype
TCMBANKDI017308 Endocrine System Diseases Abnormality of the endocrine system; Growth abnormality Pathologic Function phenotype
TCMBANKDI017773 Nutritional and Metabolic Diseases Abnormality of metabolism/homeostasis Finding phenotype
TCMBANKDI018314 Female Urogenital Diseases and Pregnancy Complications; Infections - Disease or Syndrome disease
TCMBANKDI020373 - Abnormality of the musculature Pathologic Function phenotype
TCMBANKDI020792 Endocrine System Diseases Abnormality of the endocrine system Disease or Syndrome disease
TCMBANKDI021387 Nutritional and Metabolic Diseases Abnormality of metabolism/homeostasis Disease or Syndrome phenotype