Assay Details
Target Gene Details
Entrez Gene ID: | 3990 |
Gene Name: | lipase C, hepatic type |
Gene Aliases: |
HDLCQ12, HL, HTGL, LIPH |
Location: |
Chr.15:58410754-58568952 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LIPC | XM_005254372.1 | XP_005254429.1 | ||
| AK290062.1 | ||||
| AK292631.1 | ||||
| BC146659.1 |
Target Gene Details
Entrez Gene ID: | 101928635 |
Gene Name: | uncharacterized LOC101928635 |
Gene Aliases: |
- |
Location: |
Chr.15:58106609-58431770 on Build GRCh38 |
Assay Gene Location: |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LOC101928635 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3892705 | Chr.15:58414647 - 58428232 on Build GRCh38 | Loss |
|
| nsv569598 | Chr.15:58260407 - 58560264 on Build GRCh38 | Loss |
|
| nsv1047048 | Chr.15:58409201 - 58492601 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs144155997] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
|

Genomic Map