ENSG00000128322


Homo sapiens

Features
Gene ID: ENSG00000128322
  
Biological name :IGLL1
  
Synonyms : IGLL1 / immunoglobulin lambda like polypeptide 1 / P15814
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: -1
Band: q11.23
Gene start: 23573125
Gene end: 23580308
  
Corresponding Affymetrix probe sets: 206660_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000403391
Ensembl peptide - ENSP00000249053
Ensembl peptide - ENSP00000329312
NCBI entrez gene - 3543     See in Manteia.
OMIM - 146770
RefSeq - XM_011530169
RefSeq - NM_020070
RefSeq - NM_152855
RefSeq Peptide - NP_064455
RefSeq Peptide - NP_690594
swissprot - P15814
swissprot - C9JEE0
Ensembl - ENSG00000128322
  
Related genetic diseases (OMIM): 613500 - Agammaglobulinemia 2, 613500
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 CU571382.4ENSDARG00000110539Danio rerio
 FP016018.1ENSDARG00000093689Danio rerio
 FP016018.4ENSDARG00000111019Danio rerio
 IGLL1ENSGALG00000021139Gallus gallus
 Iglc1ENSMUSG00000105906Mus musculus
 Iglc4ENSMUSG00000106039Mus musculus
 Igll1ENSMUSG00000075370Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
IGLL5 / B9A064 / immunoglobulin lambda like polypeptide 5ENSG0000025470975
IGLC2 / P0DOY2 / immunoglobulin lambda constant 2ENSG0000021167742
IGLC1 / immunoglobulin lambda constant 1ENSG0000021167541
IGLC3 / P0DOY3 / immunoglobulin lambda constant 3 (Kern-Oz+ marker)ENSG0000021167941
IGLC7 / immunoglobulin lambda constant 7ENSG0000021168541
IGKC / immunoglobulin kappa constantENSG0000021159216


Protein motifs (from Interpro)
Interpro ID Name
 IPR003006  Immunoglobulin/major histocompatibility complex, conserved site
 IPR003597  Immunoglobulin C1-set
 IPR007110  Immunoglobulin-like domain
 IPR013783  Immunoglobulin-like fold
 IPR036179  Immunoglobulin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006910 phagocytosis, recognition IBA
 biological_processGO:0006911 phagocytosis, engulfment IBA
 biological_processGO:0006955 immune response NAS
 biological_processGO:0006958 complement activation, classical pathway IBA
 biological_processGO:0042742 defense response to bacterium IBA
 biological_processGO:0045087 innate immune response IBA
 biological_processGO:0050853 B cell receptor signaling pathway IBA
 biological_processGO:0050871 positive regulation of B cell activation IBA
 biological_processGO:0050900 leukocyte migration TAS
 cellular_componentGO:0005576 extracellular region TAS
 cellular_componentGO:0009897 external side of plasma membrane IBA
 cellular_componentGO:0016020 membrane NAS
 cellular_componentGO:0042571 immunoglobulin complex, circulating IBA
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:0072562 blood microparticle IBA
 molecular_functionGO:0003823 antigen binding IBA
 molecular_functionGO:0034987 immunoglobulin receptor binding IBA


Pathways (from Reactome)
Pathway description
Cell surface interactions at the vascular wall


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000218 High palate "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428]
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 HP:0000246 Sinusitis 
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 HP:0000286 Epicanthus "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [HPO:curators]
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 HP:0000316 Hypertelorism 
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 HP:0000389 Chronic otitis media 
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 HP:0000509 Conjunctivitis "Inflammation of the conjunctiva." [HPO:curators]
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 HP:0000988 Skin rash 
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 HP:0001287 Meningitis 
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 HP:0001369 Arthritis 
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 HP:0001508 Failure to thrive 
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 HP:0001581 Recurrent skin infections "Infections of the skin that happen multiple times." [HPO:curators]
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 HP:0001875 Neutropenia 
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 HP:0001944 Dehydration 
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 HP:0001945 Fever 
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 HP:0002014 Diarrhea 
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 HP:0002024 Malabsorption 
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 HP:0002110 Bronchiectasis 
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 HP:0002205 Recurrent respiratory infections 
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 HP:0002718 Recurrent bacterial infections 
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 HP:0002721 Immunodeficiency 
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 HP:0002754 Osteomyelitis 
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 HP:0003593 Early onset 
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 HP:0004432 Agammaglobulinemia 
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 HP:0006532 Pneumonia, recurrent episodes 
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 HP:0008572 External ear malformation 
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 HP:0012115 Hepatitis "Inflammation of the liver." [HPO:probinson]
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
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 HP:0012735 Cough "A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation." [HPO:probinson]
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 HP:0100658 Cellulitis 
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 HP:0100806 Sepsis 
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 HP:0200043 verrucae "Benign growths on the skin or mucous membranes that cause cosmetic problems as well as pain and discomfort. Warts most often occur on the hands, feet, and genital areas." [HPO:SKOEHLER]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000128218 Q9UKI3 / VPREB3 / V-set pre-B cell surrogate light chain 3  / complex / reaction
 ENSG00000211899 IGHM / P01871 / immunoglobulin heavy constant mu  / reaction / complex
 ENSG00000128322 IGLL1 / P15814 / immunoglobulin lambda like polypeptide 1  / reaction / complex
 ENSG00000169575 P12018 / VPREB1 / V-set pre-B cell surrogate light chain 1  / reaction / complex






 

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