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Gene : BPIFB2 Homo sapiens

Name  ? BPI fold containing family B member 2 Cytological Location  20q11.21
Brief Description  BPI fold containing family B member 2
Description  This gene encodes a member of the lipid transfer/lipopolysaccharide binding protein (LT/LBP) gene family. It is highly expressed in hypertrophic tonsils. This gene and three other members of the LT/LBP gene family form a cluster on the long arm of chromosome 20. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HGNC:16177,
  • AF465765,
  • bactericidal/permeability-increasing protein-like 1,
  • BPIL1,
  • LPLUNC2,
  • BPIL1,
  • BPIFB2,
  • NM_025227,
  • dJ726C3.2,
  • uc002wyj.5,
  • C20orf184,
  • dJ726C3.2,
  • C20orf184,
  • LPLUNC2,
  • RYSR,
  • OTTHUMG00000032232
  • identifiers:
  • 80341,
  • ENSG00000078898,
  • BPIFB2

Genome feature

Region: gene ? Length: 16000  
Location: 20:33007704-33023703 Cyto location: 20q11.21

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



13 SN Ps

5 Cross References

14 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results