CH25H
Cholesterol 25-hydroxylase
Also known as: CH25H_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95992
- Gene
- CH25H
- Ensembl
- ENSG00000138135
- Chromosome
- 10
- Canonical length
- 272 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
OverviewNCBI Gene
This is an intronless gene that is involved in cholesterol and lipid metabolism. The encoded protein is a membrane protein and contains clusters of histidine residues essential for catalytic activity. Unlike most other sterol hydroxylases, this enzyme is a member of a small family of enzymes that utilize diiron cofactors to catalyze the hydroxylation of hydrophobic substrates. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
272 residues, UniProt reviewed canonical sequence.
>O95992|CH25H
1 MSCHNCSDPQ VLCSSGQLFL QPLWDHLRSW EALLQSPFFP VIFSITTYVG FCLPFVVLDI
61 LCSWVPALRR YKIHPDFSPS AQQLLPCLGQ TLYQHVMFVF PVTLLHWARS PALLPHEAPE
121 LLLLLHHILF CLLLFDMEFF VWHLLHHKVP WLYRTFHKVH HQNSSSFALA TQYMSVWELF
181 SLGFFDMMNV TLLGCHPLTT LTFHVVNIWL SVEDHSGYNF PWSTHRLVPF GWYGGVVHHD
241 LHHSHFNCNF APYFTHWDKI LGTLRTASVP ARLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CH25H can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 3
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- thymus: 33 nTPM
- adipose tissue: 21 nTPM
- urinary bladder: 17 nTPM
- lung: 17 nTPM
- esophagus: 14 nTPM
- gallbladder: 14 nTPM
Single-cell type
- vascular smooth muscle cells: 214 nCPM
- pericytes: 150 nCPM
- microglia: 101 nCPM
- breast lactating cells: 97 nCPM
- epididymal principal cells: 81 nCPM
- fibroblasts: 48 nCPM
Immune cell
- memory CD8 T-cell: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- medulla oblongata: 30 nTPM
- midbrain: 12 nTPM
- spinal cord: 12 nTPM
- hypothalamus: 12 nTPM
- white matter: 11 nTPM
- pons: 10 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.87
- gnomAD pLI
- 0.23
- gnomAD missense Z
- 0.38
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- B cell chemotaxis
- cholesterol metabolic process
- lipid metabolic process
- response to type I interferon
- sterol biosynthetic process
- negative regulation of cholesterol metabolic process
- negative regulation of fusion of virus membrane with host plasma membrane
Molecular functions
- C-4 methylsterol oxidase activity
- iron ion binding
- steroid hydroxylase activity
- cholesterol 25-hydroxylase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CH25H as an antibody target. Whether an autoantibody or antibody against CH25H could matter depends on whether native CH25H is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CH25H is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CH25H as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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