LIPN (lipase family member N)

2014-11-01  

Identity

HGNC
LOCATION
10q23.31
LOCUSID
ALIAS
ARCI8,LI4,LIPL4,bA186O14.3

Other Information

Locus ID:

NCBI: 643418
MIM: 613924
HGNC: 23452
Ensembl: ENSG00000204020

Variants:

dbSNP: 643418
ClinVar: 643418
TCGA: ENSG00000204020
COSMIC: LIPN

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000204020ENST00000404459Q5VXI9

Expression (GTEx)

0
5
10
15
20

Pathways

PathwaySourceExternal ID
MetabolismREACTOMER-HSA-1430728
Metabolism of lipids and lipoproteinsREACTOMER-HSA-556833
Lipid digestion, mobilization, and transportREACTOMER-HSA-73923
Digestion of dietary lipidREACTOMER-HSA-192456

References

Pubmed IDYearTitleCitations
214395402011A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.22
214395402011A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.22

Citation

Dessen P

LIPN (lipase family member N)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/66120/lipn-(lipase-family-member-n)