lipase family member N

Summary
Gene Symbol
  • LIPN
Aliases
  • bA186O14.3
Organism
Homo sapiens (human)
NCBI Gene
643418
HGNC
23452
PubChem
643418
Alliance of Genome Resources
Annotation
Keyword
  • Disulfide bond
  • Glycoprotein
  • Hydrolase
  • Ichthyosis
  • Lipid degradation
  • Proteomics identification
  • Reference proteome
  • Secreted
  • Signal
Proteins
Displaying 1 entry
UniProt Protein Name
Q5VXI9
  • Lipase-like abhydrolase domain-containing protein 4
OrthoDB (Group)
Group level
Eukaryota
Group Name
lipase
Functional Category
  • G: Carbohydrate transport and metabolism
  • I: Lipid transport and metabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
InterPro
Alpha/Beta hydrolase fold
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0060717 autosomal recessive congenital ichthyosis 8
The Human Phenotype Ontology
Displaying entries 1 - 10 of 24 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000083 Renal insufficiency
HP:0000164 Abnormality of the dentition
HP:0000232 Everted lower lip vermilion
HP:0000389 Chronic otitis media
HP:0000656 Ectropion
HP:0000958 Dry skin
HP:0000962 Hyperkeratosis
HP:0000989 Pruritus
HP:0001019 Erythroderma
Displaying all 2 entries
Disease ID Disease Name
ORPHA:313
  • autosomal recessive congenital ichthyosis 1
  • ichthyosis, congenital, autosomal recessive 14
  • lamellar ichthyosis
OMIM:613943
  • autosomal recessive congenital ichthyosis 8
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP001147
Gene Name
lipase, family member N

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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