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LMBR1

靶点ID:TCMBANKGE014352

靶点别名:ACHP; C7orf2; DIF14; LSS; PPD2; THYP; TPT; ZRS

靶点描述:limb development membrane protein 1

染色体:7

染色体位置:7q36.3

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:13243

OMIM_Link:605522

Ensembl_Link:ENSG00000105983

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

TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005587	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI006583	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI007314	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009657	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	group
TCMBANKDI011008	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI013183	Musculoskeletal Diseases	Abnormality of limbs	Anatomical Abnormality	phenotype
TCMBANKDI013615	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI013913	Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI014706	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI014928	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI016031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016221	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI017577	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI017658	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI018553	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI018888	-	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI019358	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI020739	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI023508	-	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024559	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI024595	-	-	Anatomical Abnormality	group
TCMBANKDI028951	-	-	Finding	phenotype
TCMBANKDI030837	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI030939	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031083	-	Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI031498	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype