LIPC
This page contains an overview of the genetic variation in the LIPC gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
LIPC gene and transcript details
Gene Name
lipase, hepatic
Gene Links
Ensembl: ENSG00000166035 -
Locus Reference Genomic:
Genomic Location
Chromosome 15 : 58,724,232 - 58,861,026 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1497 bases) | Protein (499 aa) |
|---|---|---|
 |
ENST00000299022 | ENSP00000299022 |
 |
||
 |
NM_000236.2 | |
 |
P11150 |
Summary of LIPC in Cardiomyopathies
LIPC variants in ExAC
Details of the protein-altering LIPC variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
| Total Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 271 | 0.00512 |
| Truncating | 20 | 0.00034 |
| Missense | 226 | 0.00418 |
| Inframe | 0 | 0.00000 |
| Splice Site | 25 | 0.00060 |