Fatty acid 2-hydroxylase

Summary
UniProt ID
Q7L5A8
Gene Symbol
FA2H FAAH FAXDC1
Gene ID
79152
Organism
Homo sapiens (human)
PubChem
Q7L5A8
SwissLipids
The Human Metabolome Database
HMDBP08645
The O-GlcNAc Database
Q7L5A8
Re-Glyco
Q7L5A8
Annotation
Keyword
Alternative splicing Disease variant Fatty acid biosynthesis Heme Hereditary spastic paraplegia Leukodystrophy Microsome Oxidoreductase Proteomics identification Reference proteome Sphingolipid metabolism Transmembrane helix Zinc
Gene Ontology (GO)
GO Hierarchy
Sequence
MAPAPPPAASFSPSEVQRRLAAGACWVRRGARLYDLSSFVRHHPGGEQLLRARAGQDISADLDGPPHRHSANARRWLEQYYVGELRGEQQGSMENEPVALEETQKTDPAMEPRFKVVDWDKDLVDWRKPLLWQVGHLGEKYDEWVHQPVTRPIRLFHSDLIEGLSKTVWYSVPIIWVPLVLYLSWSYYRTFAQGNVRLFTSFTTEYTVAVPKSMFPGLFMLGTFLWSLIEYLIHRFLFHMKPPSDSYYLIMLHFVMHGQHHKAPFDGSRLVFPPVPASLVIGVFYLCMQLILPEAVGGTVFAGGLLGYVLYDMTHYYLHFGSPHKGSYLYSLKAHHVKHHFAHQKSGFGISTKLWDYCFHTLTPEKPHLKTQ
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
158
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Sphingolipid de novo biosynthesis Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:0110786 hereditary spastic paraplegia 35

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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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Last updated: April 6, 2026