Basic Information

LIPC

Full name: lipase C, hepatic type

Gene type: protein coding

HGNC ID: HGNC:6619

Gene location: 15q21.3

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/3990

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:6619

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000236.3

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P11150

AlphaFold: https://alphafold.ebi.ac.uk/entry/P11150

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/151670

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=3990

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa00561+3990

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
LIPC AMD N/A rs10468017 C>T chr15:58386313 (GRCh38.p13)
LIPC AMD N/A rs493258 T>C chr15:58395681 (GRCh38.p13)
LIPC nAMD Missense Variant rs6078 G>A / G>T chr15:58541794 (GRCh38.p13)
LIPC nAMD Missense Variant rs6083 A>C / A>G chr15:58545811 (GRCh38.p13)
LIPC nAMD Missense Variant rs3829462 C>A / C>T chr15:58560880 (GRCh38.p13)
LIPC Drusen Area in Central Circle N/A rs920915 C>G chr15:58396268 (GRCh38.p13)
LIPC AMD N/A rs1532085 A>G / A>T chr15:58391167 (GRCh38.p13)
LIPC N/A rs1601935 G>T chr15:58379566 (GRCh38.p13)
LIPC N/A rs62001736 G>A chr15:58381852 (GRCh38.p13)
LIPC N/A rs2043082 G>A / G>C chr15:58382109 (GRCh38.p13)
LIPC N/A rs4775041 G>C chr15:58382496 (GRCh38.p13)
LIPC N/A rs80123226 A>C / A>G / A>T chr15:58383833 (GRCh38.p13)
LIPC N/A rs261290 T>C chr15:58386521 (GRCh38.p13)
LIPC N/A rs7350789 G>A chr15:58387469 (GRCh38.p13)
LIPC N/A rs58719229 delGAA chr15:58387609-58387615 (GRCh38.p13)
LIPC N/A rs261291 T>A / T>C chr15:58387979 (GRCh38.p13)
LIPC N/A rs7177289 C>G / C>T chr15:58387985 (GRCh38.p13)
LIPC N/A rs2414577 T>A / T>C chr15:58388439 (GRCh38.p13)
LIPC N/A rs2414578 T>A / T>C chr15:58388440 (GRCh38.p13)
LIPC N/A rs35853021 G>A / G>C / G>T chr15:58388444 (GRCh38.p13)
LIPC N/A rs2043085 T>C chr15:58388755 (GRCh38.p13)
LIPC Intron Variant rs35980001 dupC chr15:58430392-58430393 (GRCh38.p13)
LIPC N/A Intron Variant rs1077835 A>G chr15:58431227 (GRCh38.p13)
LIPC N/A Intron Variant rs1077834 T>A / T>C / T>G chr15:58431280 (GRCh38.p13)
LIPC Intron Variant rs1800588 C>A / C>G / C>T chr15:58431476 (GRCh38.p13)
LIPC Intron Variant rs2070895 G>A / G>T chr15:58431740 (GRCh38.p13)
LIPC SID vs. No RPD/SID Intron Variant rs12912415 A>G / A>T chr15:58429248 (GRCh38.p13)
LIPC N/A rs2043084 G>C chr15:58390297 (GRCh38.p13)