Showing entry for Immunoglobulin lambda-like polypeptide 1


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT008159
Protein NameImmunoglobulin lambda-like polypeptide 1
Uniport IdP15814
GeneIGLL1
Gene Id3543
DomainC1-set
Pfam PF07654  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
6. Human Diseases 6.3 Immune diseases hsa05340 Primary immunodeficiency
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0050853 B cell receptor signaling pathway
Biological Process GO:0006958 complement activation, classical pathway
Biological Process GO:0042742 defense response to bacterium
Biological Process GO:0006955 immune response
Biological Process GO:0045087 innate immune response
Biological Process GO:0050900 leukocyte migration
Biological Process GO:0006911 phagocytosis, engulfment
Biological Process GO:0006910 phagocytosis, recognition
Biological Process GO:0050871 positive regulation of B cell activation
molecular function GO:0003823 antigen binding
molecular function GO:0034987 immunoglobulin receptor binding
cellular component GO:0005783 endoplasmic reticulum
cellular component GO:0009897 external side of plasma membrane
cellular component GO:0005576 extracellular region
cellular component GO:0042571 immunoglobulin complex, circulating
cellular component GO:0016020 membrane
Reactome
Pathway Id Pathway Name
R-HSA-109582 Hemostasis
R-HSA-202733 Cell surface interactions at the vascular wall
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0001768 BXGD000075 Agammaglobulinemia Immune System Diseases; Hemic and Lymphatic Diseases
C0003864 BXGD000231 Arthritis Musculoskeletal Diseases
C0006267 BXGD000383 Bronchiectasis Respiratory Tract Diseases
C0007642 BXGD000469 Cellulitis Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases
C0009763 BXGD000628 Conjunctivitis Eye Diseases
C0010200 BXGD000653 Coughing Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0011175 BXGD000701 Dehydration Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0011991 BXGD000766 Diarrhea Pathological Conditions, Signs and Symptoms
C0015230 BXGD000969 Exanthema Skin and Connective Tissue Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0015695 BXGD001013 Fatty Liver Digestive System Diseases
C0015967 BXGD001030 Fever Pathological Conditions, Signs and Symptoms
C0019158 BXGD001293 Hepatitis Digestive System Diseases
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0024523 BXGD001781 Malabsorption Syndrome Digestive System Diseases; Nutritional and Metabolic Diseases
C0025289 BXGD001851 Meningitis Nervous System Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0027947 BXGD002061 Neutropenia Hemic and Lymphatic Diseases
C0029443 BXGD002152 Osteomyelitis Infections; Musculoskeletal Diseases
C0037199 BXGD002671 Sinusitis Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0043037 BXGD003023 Common wart Neoplasms; Infections; Skin and Connective Tissue Diseases
C0085404 BXGD003166 POEMS Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
C0086438 BXGD003283 Hypogammaglobulinemia Immune System Diseases; Hemic and Lymphatic Diseases
C0221026 BXGD004371 X-linked agammaglobulinemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
C0240635 BXGD005047 Byzanthine arch palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
C0243026 BXGD005210 Sepsis Pathological Conditions, Signs and Symptoms; Infections
C0266589 BXGD005698 Congenital ear anomaly NOS (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Otorhinolaryngologic Diseases
C0271441 BXGD006203 Chronic otitis media Otorhinolaryngologic Diseases
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0678230 BXGD009750 Congenital Epicanthus
C0694550 BXGD009852 Recurrent pneumonia Infections; Respiratory Tract Diseases
C1292769 BXGD012230 Precursor B-cell lymphoblastic leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1832241 BXGD013813 Agammaglobulinemia, non-Bruton type Immune System Diseases; Hemic and Lymphatic Diseases
C1844383 BXGD014628 Recurrent bacterial infection Infections
C1846460 BXGD014820 Abnormality of the outer ear
C1853193 BXGD015312 Recurrent skin infections Infections; Skin and Connective Tissue Diseases
C1963165 BXGD016685 Malabsorption, CTCAE
C2711227 BXGD017478 Steatohepatitis Digestive System Diseases
C2985280 BXGD018223 Blood Protein Measurement
C3150750 BXGD018332 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE
C3665596 BXGD019295 Warts Infections; Skin and Connective Tissue Diseases
C3714745 BXGD019427 Malabsorption Digestive System Diseases
C3806482 BXGD019514 Recurrent respiratory infections Infections; Respiratory Tract Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002616 Copper 63.55
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