lipase H

Summary
Gene Symbol
  • LIPH
Aliases
  • LPDLR
  • PLA1B
  • mPA-PLA1
  • mPA-PLA1alpha
  • phospholipase A(1)
Organism
Homo sapiens (human)
NCBI Gene
200879
HGNC
18483
PubChem
200879
Alliance of Genome Resources
Annotation
Keyword
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Heparin-binding
  • Hydrolase
  • Hypotrichosis
  • Lipid degradation
  • Proteomics identification
  • Reference proteome
  • Secreted
  • Signal
Proteins
Displaying all 2 entries
UniProt Protein Name
A2IBA6
Q8WWY8
  • LPD lipase-related protein
  • Membrane-associated phosphatidic acid-selective phospholipase A1-alpha
  • Phospholipase A1 member B
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
lipase I
Functional Category
  • I: Lipid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Displaying all 2 entries
Gene Ontology
lipase activity
lipid metabolic process
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0110704 hypotrichosis 7
The Human Phenotype Ontology
Displaying entries 1 - 10 of 23 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000164 Abnormality of the dentition
HP:0000479 Abnormal retinal morphology
HP:0000486 Strabismus
HP:0000518 Cataract
HP:0000615 Abnormal pupil morphology
HP:0000653 Sparse eyelashes
HP:0000951 Abnormality of the skin
HP:0000971 Abnormal sweat gland morphology
HP:0001596 Alopecia
Displaying all 3 entries
Disease ID Disease Name
ORPHA:170
  • isolated familial wooly hair disorder
ORPHA:55654
  • hypotrichosis simplex
OMIM:604379
  • hypotrichosis 7
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP001838
Gene Name
lipase, member H

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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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