Homo sapiens Protein: IGLL1
Summary
InnateDB Protein IDBP-2437.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol IGLL1
Protein Name immunoglobulin lambda-like polypeptide 1
Synonyms 14.1; AGM2; CD179b; IGL1; IGL5; IGLJ14.1; IGLL; IGO; IGVPB; VPREB2;
Species Homo sapiens
Ensembl Protein ENSP00000249053
InnateDB Gene IDBG-2433 (IGLL1)
Protein Structure
UniProt Annotation
Function Critical for B-cell development. {ECO:0000269PubMed:9419212}.
Subcellular Localization Secreted {ECO:0000269PubMed:9419212}.
Disease Associations Agammaglobulinemia 2, autosomal recessive (AGM2) [MIM:613500]: A primary immunodeficiency characterized by profoundly low or absent serum antibodies and low or absent circulating B cells due to an early block of B-cell development. Affected individuals develop severe infections in the first years of life. {ECO:0000269PubMed:9419212}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed only in pre-B-cells and a special B- cell line (which is surface Ig negative). {ECO:0000269PubMed:2128466}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0006955 immune response
Cellular Component
GO:0016020 membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P15814
PhosphoSite PhosphoSite-P15814
TrEMBL
UniProt Splice Variant
Entrez Gene 3543
UniGene Hs.348935
RefSeq NP_690594
HUGO HGNC:5870
OMIM 146770
CCDS CCDS13810
HPRD 00905
IMGT
EMBL AP000345 BC012293 BC030239 M27749 M34511 M34512 M34513 X03528 X03530
GenPept AAA36096 AAA36100 AAH12293 AAH30239 CAA27229 CAA27231