Showing entry for Astrotactin-2


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT005101
Protein NameAstrotactin-2
Uniport IdO75129
GeneASTN2
Gene Id23245
DomainAnnexin_like; ASTN_2_hairpin; FXa_inhibition; MACPF
Pfam PF18411   PF18577   PF01823  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0048105 establishment of body hair planar orientation
Biological Process GO:2000009 negative regulation of protein localization to cell surface
Biological Process GO:0007158 neuron cell-cell adhesion
Biological Process GO:0001764 neuron migration
Biological Process GO:0015031 protein transport
molecular function GO:0005509 calcium ion binding
molecular function GO:0043533 inositol 1,3,4,5 tetrakisphosphate binding
cellular component GO:0005938 cell cortex
cellular component GO:0060187 cell pole
cellular component GO:0030136 clathrin-coated vesicle
cellular component GO:0005769 early endosome
cellular component GO:0005768 endosome
cellular component GO:0016021 integral component of membrane
cellular component GO:0005770 late endosome
cellular component GO:0043204 perikaryon
Reactome
Pathway Id Pathway Name
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002395 BXGD000111 Alzheimer's Disease Nervous System Diseases; Mental Disorders
C0004352 BXGD000269 Autistic Disorder Mental Disorders
C0004936 BXGD000295 Mental disorders Mental Disorders
C0005586 BXGD000315 Bipolar Disorder Mental Disorders
C0005890 BXGD000345 Body Height
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0009241 BXGD000595 Cognition Disorders Mental Disorders
C0011265 BXGD000708 Presenile dementia Nervous System Diseases; Mental Disorders
C0014175 BXGD000904 Endometriosis Female Urogenital Diseases and Pregnancy Complications
C0016529 BXGD001068 Forced expiratory volume function
C0017654 BXGD001136 Glomerular Filtration Rate
C0018681 BXGD001214 Headache Pathological Conditions, Signs and Symptoms
C0023508 BXGD001675 White Blood Cell Count procedure
C0024117 BXGD001734 Chronic Obstructive Airway Disease Respiratory Tract Diseases
C0026848 BXGD001941 Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0029410 BXGD002138 Osteoarthritis of hip Musculoskeletal Diseases
C0035227 BXGD002514 Respiratory Function Tests
C0036341 BXGD002600 Schizophrenia Mental Disorders
C0042834 BXGD003004 Vital capacity
C0149931 BXGD003388 Migraine Disorders Nervous System Diseases
C0201976 BXGD004063 Creatinine measurement, serum (procedure)
C0205682 BXGD004105 Waist-Hip Ratio
C0233514 BXGD004584 Abnormal behavior Behavior and Behavior Mechanisms
C0234985 BXGD004708 Mental deterioration Mental Disorders
C0235974 BXGD004796 Pancreatic carcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0236733 BXGD004822 Amphetamine-Related Disorders Chemically-Induced Disorders; Mental Disorders
C0236773 BXGD004827 Depressed bipolar I disorder Mental Disorders
C0236804 BXGD004835 Amphetamine Addiction Chemically-Induced Disorders; Mental Disorders
C0236807 BXGD004836 Amphetamine Abuse Chemically-Induced Disorders; Mental Disorders
C0241005 BXGD005072 Creatine phosphokinase serum increased
C0270968 BXGD006143 Limb-girdle muscular dystrophy type 2H Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0338480 BXGD007186 Common Migraine Nervous System Diseases
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0410702 BXGD008447 Adolescent idiopathic scoliosis Musculoskeletal Diseases
C0428883 BXGD008639 Diastolic blood pressure
C0497327 BXGD009061 Dementia Nervous System Diseases; Mental Disorders
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0686353 BXGD009833 Muscular Dystrophies, Limb-Girdle Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0752166 BXGD010684 Bardet-Biedl Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
C0869220 BXGD011305 Adverse effects, not elsewhere classified
C0871470 BXGD011316 Systolic Pressure
C1263846 BXGD011897 Attention deficit hyperactivity disorder Mental Disorders
C1269683 BXGD012001 Major Depressive Disorder Mental Disorders
C1510586 BXGD013176 Autism Spectrum Disorders Mental Disorders
C1518922 BXGD013229 peak expiratory flow (procedure)
C1535926 BXGD013322 Neurodevelopmental Disorders Mental Disorders
C1837461 BXGD014234 SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
C1859569 BXGD015911 BARDET-BIEDL SYNDROME 11 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
C4277682 BXGD022376 Chemical and Drug Induced Liver Injury Digestive System Diseases; Chemically-Induced Disorders
C4721579 BXGD023759 Secondary malignant neoplasm of colon and/or rectum Digestive System Diseases; Neoplasms
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0018397 beta-1,4-mannan 180.06
BXGC0050194 alpha-D-Mannose 180.06
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein