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NALCN

靶点ID:TCMBANKGE010067

靶点别名:CLIFAHDD; CanIon; IHPRF; IHPRF1; INNFD; VGCNL1; bA430M15.1

靶点描述:sodium leak channel, non-selective

染色体:13

染色体位置:13q32.3-q33.1

靶点类型:protein-coding

HERB_ID:-

HGNC_Link:19082

OMIM_Link:611549

Ensembl_Link:ENSG00000102452

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

TCMBANKIN008636	acetylcholine	Vagusstoff; AC1NSTAT; Acetylcholine Hydroxide; 2-acetyloxyethyl(trimethyl)azanium hydroxide; SCHEMBL3904052; 56-13-3	C7H16NO2+	146.21 g/mol	CC(=O)OCC[N+](C)(C)C
TCMBANKIN061617	eugenol 4-Allyl-2-methoxyphenol		C10H12O2		COC1=C(C=CC(=C1)CC=C)O

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI000590	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases	Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI001342	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI002572	-	-	Finding	disease
TCMBANKDI002606	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI002718	-	-	Finding	phenotype
TCMBANKDI002779	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI002881	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI003879	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases	Abnormality of the genitourinary system	Congenital Abnormality	disease
TCMBANKDI004145	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	group
TCMBANKDI004489	-	Abnormality of the ear	Congenital Abnormality	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
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007043	Musculoskeletal Diseases	Abnormality of the skeletal system	Congenital Abnormality	disease
TCMBANKDI007228	-	-	Finding	phenotype
TCMBANKDI007610	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI007770	Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases	Abnormality of the respiratory system	Sign or Symptom	phenotype
TCMBANKDI008156	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI009575	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011744	-	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Congenital Abnormality	disease
TCMBANKDI012319	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013067	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI013148	Respiratory Tract Diseases; Nervous System Diseases	Abnormality of the nervous system; Abnormality of the respiratory system	Disease or Syndrome	disease
TCMBANKDI013169	-	Abnormality of the skeletal system	Anatomical Abnormality	disease
TCMBANKDI013728	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI013927	Respiratory Tract Diseases	Abnormality of the respiratory system	Pathologic Function	phenotype
TCMBANKDI014091	-	-	Disease or Syndrome	disease
TCMBANKDI015485	Mental Disorders	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI016031	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of limbs	Congenital Abnormality	disease
TCMBANKDI016086	-	Abnormality of the integument; Abnormality of limbs	Finding	phenotype
TCMBANKDI017965	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI018239	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI018962	Nervous System Diseases	-	Disease or Syndrome	disease
TCMBANKDI020373	-	Abnormality of the musculature	Pathologic Function	phenotype
TCMBANKDI022380	Female Urogenital Diseases and Pregnancy Complications	Abnormality of prenatal development or birth	Pathologic Function	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024559	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI024934	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases	Abnormality of head or neck	Congenital Abnormality	group
TCMBANKDI025924	-	Abnormality of limbs; Abnormality of the skeletal system	Sign or Symptom	phenotype
TCMBANKDI027274	-	Abnormality of head or neck	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
TCMBANKDI027721	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature	Disease or Syndrome	disease
TCMBANKDI029280	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI030017	-	Abnormality of the ear	Anatomical Abnormality	disease
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI031899	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases	-	Disease or Syndrome; Congenital Abnormality	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease
TCMBANKDI032419	-	Growth abnormality	Finding	phenotype