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SHOC2

靶点ID:TCMBANKGE003060

靶点别名:SIAA0862; SOC2; SUR8

靶点描述:SHOC2 leucine rich repeat scaffold protein

染色体:10

染色体位置:10q25.2

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:15454

OMIM_Link:602775

Ensembl_Link:ENSG00000108061

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

TCMBANKIN021186	hexitol	Allitol; ZINC03831017; InChI=1/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H; 488-44-8; (2R,3R,4S,5S)-hexane-1,2,3,4,5,6-hexol; GALACTITOL (D)	C6H14O6	182.17	C(C(C(C(C(CO)O)O)O)O)O
TCMBANKIN060958	oleic acid;cis-oleic acid;oleinic acid		C18H34O2	282.46	CCCCCCCCC=CCCCCCCCC(=O)O

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
TCMBANKDI000166	-	-	Neoplastic Process	disease
TCMBANKDI001016	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI003353	Pathological Conditions, Signs and Symptoms; Neoplasms	-	Neoplastic Process	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004046	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI006182	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI009697	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI009702	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	phenotype
TCMBANKDI009827	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI009912	Pathological Conditions, Signs and Symptoms	Abnormality of metabolism/homeostasis	Sign or Symptom	phenotype
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI015452	Neoplasms; Endocrine System Diseases	Abnormality of the endocrine system; Neoplasm	Neoplastic Process	disease
TCMBANKDI017024	Neoplasms; Respiratory Tract Diseases	-	Neoplastic Process	disease
TCMBANKDI020826	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders	-	Disease or Syndrome	disease
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI023140	Neoplasms; Endocrine System Diseases	Abnormality of the endocrine system; Neoplasm	Neoplastic Process	disease
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024535	Neoplasms; Respiratory Tract Diseases	Neoplasm; Abnormality of the respiratory system	Neoplastic Process	disease
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI026008	-	-	Disease or Syndrome	disease
TCMBANKDI028305	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI029701	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI030041	Hemic and Lymphatic Diseases	-	Neoplastic Process	disease