Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55600
Gene name Gene Name - the full gene name approved by the HGNC.
Intelectin 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ITLN1
Synonyms (NCBI Gene) Gene synonyms aliases
HL-1, HL1, INTL, ITLN, LFR, hIntL, omentin
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1074506 hsa-miR-1323 CLIP-seq
MIRT1074507 hsa-miR-1470 CLIP-seq
MIRT1074508 hsa-miR-188-3p CLIP-seq
MIRT1074509 hsa-miR-4667-3p CLIP-seq
MIRT1074510 hsa-miR-532-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001934 Process Positive regulation of protein phosphorylation IDA 16531507
GO:0005509 Function Calcium ion binding IDA 26148048
GO:0005515 Function Protein binding IPI 26819645
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609873 18259 ENSG00000179914
Protein
UniProt ID Q8WWA0
Protein name Intelectin-1 (ITLN-1) (Endothelial lectin HL-1) (Galactofuranose-binding lectin) (Intestinal lactoferrin receptor) (Omentin)
Protein function Lectin that specifically recognizes microbial carbohydrate chains in a calcium-dependent manner (PubMed:11313366, PubMed:26148048). Binds to microbial glycans that contain a terminal acyclic 1,2-diol moiety, including beta-linked D-galactofurano
PDB 4WMQ , 4WMY , 6USC
Family and domains
Tissue specificity TISSUE SPECIFICITY: Highly expressed in omental adipose tissue where it is found in stromal vascular cells but not in fat cells but is barely detectable in subcutaneous adipose tissue (at protein level) (PubMed:16531507). Highly expressed in the small int
Sequence
MNQLSFLLFLIATTRGWSTDEANTYFKEWTCSSSPSLPRSCKEIKDECPSAFDGLYFLRT
ENGVIYQTFCDMTSGGGGWTLVASVHENDMRGKCTVGDRWSSQQGSKAVYPEGDGNWANY
NTFGSAEAATSDDYKNPGYYDIQAKDLGIWHVPNKSPMQHWRNSSLLRYRTDTGFLQTLG
HNLFGIYQKYPVKYGEGKCWTDNGPVIPVVYDFGDAQKTASYYSPYGQREFTAGFVQFRV
FNNERAANALCAGMRVTGCNTEHHCIGGGGYFPEASPQQCGDFSGFDWSGYGTHVGYSSS
REITEAAVLLFYR
Sequence length 313
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Antimicrobial peptides
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Crohn Disease Crohn's disease N/A N/A GWAS
Inflammatory Bowel Disease Inflammatory bowel disease N/A N/A GWAS
Lung adenocarcinoma Familial squamous cell lung carcinoma N/A N/A GWAS
Ulcerative colitis Ulcerative colitis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Psoriatic Stimulate 23144698
Asthma Associate 35550122
Atherosclerosis Associate 33054020, 36224302
Axial Spondyloarthritis Associate 32541676
Barrett Esophagus Associate 30323168
Cachexia Associate 32232960
Carcinoma Hepatocellular Inhibit 38050235
Cardiomyopathies Inhibit 28687077
Cardiovascular Diseases Associate 32541676
Celiac Disease Associate 28934294