Fatty acid 2-hydroxylase

Summary
UniProt ID
Q7L5A8
Gene Symbol
  • FA2H
  • FAAH
  • FAXDC1
Organism
Homo sapiens (human)
PubChem
Q7L5A8
SwissLipids
The Human Metabolome Database
HMDBP08645
The O-GlcNAc Database
Q7L5A8
Annotation
Keyword
  • Alternative splicing
  • Disease variant
  • Fatty acid biosynthesis
  • Heme
  • Hereditary spastic paraplegia
  • Leukodystrophy
  • Microsome
  • Oxidoreductase
  • Reference proteome
  • Sphingolipid metabolism
  • Transmembrane helix
  • Zinc
Gene Ontology (GO)
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

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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: December 9, 2024