cytochrome P450 family 39 subfamily A member 1

Summary
Gene Symbol
  • CYP39A1
Organism
Homo sapiens (human)
External Links
NCBI Gene
51302
HGNC
17449
KEGG Gene ID
hsa:51302
PubChem
51302
Alliance of Genome Resources
Annotation
Keyword
  • Cholesterol metabolism
  • Heme
  • Microsome
  • Monooxygenase
  • Proteomics identification
  • Reference proteome
  • Signal
  • Steroid metabolism
  • Transmembrane
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
Q9NYL5
  • Cytochrome P450 39A1
  • Oxysterol 7-alpha-hydroxylase
B7Z786
A0A087WTD2
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K07439
Name
24-hydroxycholesterol 7alpha-hydroxylase [EC:1.14.14.26]
References
Disease
Disease Ontology
Displaying entries 11 - 20 of 72 in total
DO ID Disease Name Source
DOID:0110767 hereditary spastic paraplegia 14
DOID:0110768 hereditary spastic paraplegia 15
DOID:0110769 hereditary spastic paraplegia 16
DOID:0110770 hereditary spastic paraplegia 17
DOID:0110771 hereditary spastic paraplegia 18
DOID:0110772 hereditary spastic paraplegia 19
DOID:0110773 hereditary spastic paraplegia 2
DOID:0110774 hereditary spastic paraplegia 23
DOID:0110775 hereditary spastic paraplegia 24
DOID:0110776 hereditary spastic paraplegia 25
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP001831
Gene Name
cytochrome P450, family 39, subfamily A, polypeptide 1

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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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