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 1 - 10 of 72 in total
DO ID Disease Name Source
DOID:0050590 severe congenital neutropenia
DOID:0050886 Troyer syndrome
DOID:0060245 Mast syndrome
DOID:0060246 MASA syndrome
DOID:0060491 SPOAN syndrome
DOID:0080067 Charcot-Marie-Tooth disease type 5
DOID:0110763 hereditary spastic paraplegia 10
DOID:0110764 hereditary spastic paraplegia 11
DOID:0110765 hereditary spastic paraplegia 12
DOID:0110766 hereditary spastic paraplegia 13
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP001831
Gene Name
cytochrome P450, family 39, subfamily A, polypeptide 1

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024