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 21 - 30 of 72 in total
DO ID Disease Name Source
DOID:0110777 hereditary spastic paraplegia 26
DOID:0110778 hereditary spastic paraplegia 27
DOID:0110779 hereditary spastic paraplegia 28
DOID:0110780 hereditary spastic paraplegia 29
DOID:0110781 hereditary spastic paraplegia 30
DOID:0110782 hereditary spastic paraplegia 31
DOID:0110783 hereditary spastic paraplegia 32
DOID:0110785 hereditary spastic paraplegia 34
DOID:0110786 hereditary spastic paraplegia 35
DOID:0110787 hereditary spastic paraplegia 36
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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