Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3929
Gene name Gene Name - the full gene name approved by the HGNC.
Lipopolysaccharide binding protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LBP
Synonyms (NCBI Gene) Gene synonyms aliases
BPIFD2
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q11.23
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is involved in the acute-phase immunologic response to gram-negative bacterial infections. Gram-negative bacteria contain a glycolipid, lipopolysaccharide (LPS), on their outer cell wall. Together with bactericidal permeab
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017289 hsa-miR-335-5p Microarray 18185580
MIRT050450 hsa-miR-22-3p CLASH 23622248
MIRT045133 hsa-miR-186-5p CLASH 23622248
MIRT1105367 hsa-miR-4299 CLIP-seq
MIRT1105368 hsa-miR-4709-3p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
JUN Repression 15114678
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001530 Function Lipopolysaccharide binding IBA 21873635
GO:0001530 Function Lipopolysaccharide binding IDA 12594207
GO:0001530 Function Lipopolysaccharide binding IMP 24120359
GO:0001530 Function Lipopolysaccharide binding ISS 2477488
GO:0002224 Process Toll-like receptor signaling pathway TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
151990 6517 ENSG00000129988
Protein
UniProt ID P18428
Protein name Lipopolysaccharide-binding protein (LBP)
Protein function Plays a role in the innate immune response. Binds to the lipid A moiety of bacterial lipopolysaccharides (LPS), a glycolipid present in the outer membrane of all Gram-negative bacteria (PubMed:24120359, PubMed:7517398). Acts as an affinity enhan
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01273 LBP_BPI_CETP 38 212 LBP / BPI / CETP family, N-terminal domain Family
PF02886 LBP_BPI_CETP_C 241 478 LBP / BPI / CETP family, C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in blood serum (at protein level). {ECO:0000269|PubMed:2402637, ECO:0000269|PubMed:24120359}.
Sequence
Sequence length 481
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
AA amyloidosis Inhibit 28851981
Acute Aortic Syndrome Associate 32256857
Amyotrophic Lateral Sclerosis Stimulate 37350306
Arthritis Rheumatoid Associate 32404914, 34458379
Ascites Stimulate 27112233
Asthma Associate 37438758
Attention Deficit Disorder with Hyperactivity Stimulate 37199526
Autism Spectrum Disorder Stimulate 37199526
Axial Spondyloarthritis Stimulate 34560894
Bacteremia Associate 18056482