Overview

Variant ID 11930
Entrez Gene ID 4023
Gene LPL (GeneCards)
Location hg19 8:19856291-19856291
hg38 8:19998780-19998780
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000008.10:g.19856291 A>G (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 146364022

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.4909
CADD Raw score (version 1.3) -0.270889 (Deleterious)
FATHMM raw prediction score 0.08381 (Tolerated)
Deleterious probability by DeFine 0.3909 (Neutral)
Entrez Gene ID 4023 (NCBI Gene)
Official Gene Symbol LPL (GeneCards)
Number of variants in LPL in this database 4 (view all the variants)
Full name lipoprotein lipase
Band 8p21.3
Other IDs Vega: OTTHUMG00000036645
OMIM: 609708
HGNC: HGNC:6677
Ensembl: ENSG00000175445
Other names LIPD, HDLCQ11
Summary LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.08 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;