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ROM1

靶点ID:TCMBANKGE015052

靶点别名:ROM; ROSP1; RP7; TSPAN23

靶点描述:retinal outer segment membrane protein 1

染色体:11

染色体位置:11q12.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:10254

OMIM_Link:180721

Ensembl_Link:ENSG00000149489

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

TCMBANKIN003665	evoden				C1CCN(CC1)CCOC2=CC=C(C=C2)C(=O)C3=C(SC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O

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
TCMBANKDI000510	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI001068	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases	-	Disease or Syndrome	disease
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI003248	Nutritional and Metabolic Diseases; Endocrine System Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI009877	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Finding	phenotype
TCMBANKDI009912	Pathological Conditions, Signs and Symptoms	Abnormality of metabolism/homeostasis	Sign or Symptom	phenotype
TCMBANKDI011094	Musculoskeletal Diseases	-	Acquired Abnormality	disease
TCMBANKDI011446	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Congenital Abnormality	disease
TCMBANKDI013348	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI013913	Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI014608	Musculoskeletal Diseases	-	Acquired Abnormality	phenotype
TCMBANKDI015193	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases	Constitutional symptom	Sign or Symptom	phenotype
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI019586	Eye Diseases	Abnormality of metabolism/homeostasis; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI020293	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI022768	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI024668	Musculoskeletal Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI024946	-	Abnormality of the eye	Finding	phenotype
TCMBANKDI026106	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI027289	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms	-	Mental or Behavioral Dysfunction	disease
TCMBANKDI028799	Eye Diseases	-	Disease or Syndrome	disease
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI032420	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Acquired Abnormality	phenotype
TCMBANKDI032498	Nutritional and Metabolic Diseases	Abnormality of metabolism/homeostasis; Abnormality of the endocrine system	Disease or Syndrome	disease