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FKRP

靶点ID:TCMBANKGE000030

靶点别名:FKTR; LGMD2I; LGMDR9; MDC1C; MDDGA5; MDDGB5; MDDGC5

靶点描述:fukutin related protein

染色体:19

染色体位置:19q13.32

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:17997

OMIM_Link:606596

Ensembl_Link:ENSG00000181027

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

TCMBANKDI000121	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI000248	Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI002606	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI002791	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI003394	Pathological Conditions, Signs and Symptoms	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI003697	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004280	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	disease
TCMBANKDI004646	Nervous System Diseases	Abnormality of the nervous system	Disease or Syndrome	disease
TCMBANKDI005037	-	Abnormality of the eye	Anatomical Abnormality	disease
TCMBANKDI005226	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI005279	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI005528	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI006165	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007211	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI007343	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	-	Finding	phenotype
TCMBANKDI007994	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI009594	-	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI009657	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	group
TCMBANKDI009751	-	-	Finding	phenotype
TCMBANKDI009870	-	Abnormality of the voice	Finding	disease
TCMBANKDI009935	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI010717	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	-	Congenital Abnormality	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011779	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI011867	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI012128	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI012321	-	Abnormality of the nervous system	Sign or Symptom	phenotype
TCMBANKDI013873	-	Abnormality of metabolism/homeostasis	Finding	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI013994	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI016840	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI017741	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI017895	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	-	Congenital Abnormality	disease
TCMBANKDI018649	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI019508	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI019748	Musculoskeletal Diseases	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI020119	Mental Disorders	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI020257	Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI020574	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Stomatognathic Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI022150	-	-	Finding	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI023760	-	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024159	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Sign or Symptom	phenotype
TCMBANKDI024183	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI024199	-	Abnormality of limbs; Abnormality of the skeletal system; Abnormality of the musculature	Finding	phenotype
TCMBANKDI024451	-	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI024668	Musculoskeletal Diseases; Stomatognathic Diseases	-	Disease or Syndrome	disease
TCMBANKDI027248	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI027326	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Congenital Abnormality	group
TCMBANKDI027961	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases	Abnormality of the nervous system	Congenital Abnormality	disease
TCMBANKDI028085	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI028664	-	-	Finding	phenotype
TCMBANKDI028908	Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	phenotype
TCMBANKDI030579	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI030733	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI030915	-	-	Disease or Syndrome	disease
TCMBANKDI031438	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031644	Musculoskeletal Diseases	Abnormality of limbs; Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI032275	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Anatomical Abnormality	disease