Showing entry for Protein unc-119 homolog A


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT024144
Protein NameProtein unc-119 homolog A
Uniport IdQ13432
GeneUNC119
Gene Id9094
DomainGMP_PDE_delta
Pfam PF05351  
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:0007268 chemical synaptic transmission
Biological Process GO:0006897 endocytosis
Biological Process GO:0042953 lipoprotein transport
Biological Process GO:0000281 mitotic cytokinesis
Biological Process GO:2001287 negative regulation of caveolin-mediated endocytosis
Biological Process GO:1900186 negative regulation of clathrin-dependent endocytosis
Biological Process GO:0007399 nervous system development
Biological Process GO:0007602 phototransduction
Biological Process GO:0061098 positive regulation of protein tyrosine kinase activity
Biological Process GO:0007601 visual perception
molecular function GO:0008289 lipid binding
cellular component GO:0005813 centrosome
cellular component GO:0005829 cytosol
cellular component GO:0045171 intercellular bridge
cellular component GO:0051233 spindle midzone
cellular component GO:0000922 spindle pole
cellular component GO:0045202 synapse
Reactome
Pathway Id Pathway Name
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002736 BXGD000127 Amyotrophic Lateral Sclerosis Nutritional and Metabolic Diseases; Nervous System Diseases
C0009398 BXGD000604 Color vision defect Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0015397 BXGD000983 Disorder of eye Eye Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0024115 BXGD001732 Lung diseases Respiratory Tract Diseases
C0024312 BXGD001766 Lymphopenia Immune System Diseases; Hemic and Lymphatic Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0028077 BXGD002069 Nyctalopia Eye Diseases
C0032285 BXGD002344 Pneumonia Infections; Respiratory Tract Diseases
C0035309 BXGD002530 Retinal Diseases Eye Diseases
C0035334 BXGD002539 Retinitis Pigmentosa Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0085636 BXGD003218 Photophobia Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0206744 BXGD004286 T-Lymphocytopenia, Idiopathic CD4-Positive Immune System Diseases; Hemic and Lymphatic Diseases
C0220630 BXGD004302 Adult Liver Carcinoma Digestive System Diseases; Neoplasms
C0242770 BXGD005194 Bronchiolitis Obliterans Organizing Pneumonia Respiratory Tract Diseases
C0279000 BXGD006622 Liver and Intrahepatic Biliary Tract Carcinoma Digestive System Diseases; Neoplasms
C0345904 BXGD007745 Malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0494261 BXGD009023 Combined immunodeficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
C0581354 BXGD009561 Recurrent sinusitis Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0747085 BXGD010158 Recurrent otitis media Otorhinolaryngologic Diseases
C0751072 BXGD010312 Frontotemporal Lobar Degeneration Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
C1269955 BXGD012005 Tumor Cell Invasion
C1854065 BXGD015379 LATE-ONSET RETINAL DEGENERATION (disorder) Eye Diseases
C1862475 BXGD016132 Abnormality of retinal pigmentation
C1998028 BXGD016865 Photoreceptor degeneration Eye Diseases
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C3489532 BXGD018934 Cone-Rod Dystrophy 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C3665347 BXGD019279 Visual Impairment Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C3809768 BXGD019610 IMMUNODEFICIENCY 13
C3809776 BXGD019611 Recurrent shingles
C4085590 BXGD022119 Cone-Rod Dystrophies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C4277690 BXGD022377 Ciliopathies Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C4551714 BXGD023398 Rod-Cone Dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000436 Glycerol 92.09
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