Gene Gene information from NCBI Gene database.
Entrez ID 338328
Gene name Glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1
Gene symbol GPIHBP1
Synonyms (NCBI Gene)
GPI-HBP1HYPL1D
Chromosome 8
Chromosome location 8q24.3
Summary This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) f
SNPs SNP information provided by dbSNP.
8
SNP ID Visualize variation Clinical significance Consequence
rs145844329 G>A,C Pathogenic-likely-pathogenic, likely-benign Coding sequence variant, missense variant, intron variant
rs587777637 A>C Pathogenic Missense variant, coding sequence variant
rs587777638 G>A,C Pathogenic Missense variant, coding sequence variant
rs587777639 T>C,G Pathogenic Missense variant, coding sequence variant
rs587777640 G>T Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
133
miRTarBase ID miRNA Experiments Reference
MIRT017452 hsa-miR-335-5p Microarray 18185580
MIRT458115 hsa-miR-8080 PAR-CLIP 23592263
MIRT458114 hsa-miR-552-3p PAR-CLIP 23592263
MIRT458113 hsa-miR-1197 PAR-CLIP 23592263
MIRT458112 hsa-miR-4434 PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
37
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 20124439, 30559189, 32814053
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612757 24945 ENSG00000277494
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IV16
Protein name Glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPI-HBP1) (GPI-anchored HDL-binding protein 1) (High density lipoprotein-binding protein 1)
Protein function Mediates the transport of lipoprotein lipase LPL from the basolateral to the apical surface of endothelial cells in capillaries (By similarity). Anchors LPL on the surface of endothelial cells in the lumen of blood capillaries (By similarity). P
PDB 6E7K , 6OAU , 6OAZ , 6OB0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00021 UPAR_LY6 65 137 u-PAR/Ly-6 domain Domain
Sequence
MKALGAVLLALLLCGRPGRGQTQQEEEEEDEDHGPDDYDEEDEDEVEEEETNRLPGGRSR
VLLRCYTCKSLPRDERCNLTQNCSHGQTCTTLIAHGNTESGLLTTHSTWCTDSCQPITKT
VEGTQVTMTCCQSSLCN
VPPWQSSRVQDPTGKGAGGPRGSSETVGAALLLNLLAGLGAMG
ARRP
Sequence length 184
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Post-translational modification: synthesis of GPI-anchored proteins
Assembly of active LPL and LIPC lipase complexes
Chylomicron remodeling
Retinoid metabolism and transport
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
123
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cardiovascular phenotype Pathogenic rs776388699 RCV005841985
Hyperlipoproteinemia, type 1D Likely pathogenic; Pathogenic rs752728823, rs587777637, rs587777638, rs587777639, rs587777640, rs587777641, rs587777642, rs587777643, rs2130672651, rs1300685456, rs2488909361, rs780340378, rs1284611659 RCV001333096
RCV000133522
RCV000133523
RCV000133524
RCV000133526
RCV000133527
RCV000133528
RCV000133529
RCV000133530
RCV002250027
RCV002251224
RCV002468529
RCV001175121
RCV001253052
Hyperlipoproteinemia, type I Pathogenic rs587777638 RCV004576921
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cholangiocarcinoma Likely benign rs199622782 RCV005912089
Gastric cancer Uncertain significance rs147455726 RCV005895892
GPIHBP1-related disorder Conflicting classifications of pathogenicity; Benign; Likely benign rs201685731, rs78367243, rs142959160, rs145844329, rs201256271, rs546710267, rs775697635, rs545434518 RCV003941025
RCV003921324
RCV003958617
RCV003415969
RCV003923727
RCV003896160
RCV003899463
RCV003938591
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Atherosclerosis Associate 23831619
Breast Neoplasms Associate 31182966
Colitis Associate 24614124
Coronary Artery Disease Associate 23831619
Familial hyperchylomicronemia syndrome Associate 27403930, 29659879, 36613909
Hyperlipidemias Associate 24646025
Hyperlipoproteinemia Type I Associate 22008945, 23831619, 24847059, 26079787, 29288010, 29748148, 32375710, 36978188
Hypertriglyceridemia Associate 22008945, 23831619, 24614124, 24847059, 26079787, 29910226, 29921298, 30885219, 32115487, 36613909, 37981531
Hypertriglyceridemic Waist Associate 24847059
Immunologic Deficiency Syndromes Inhibit 22008945