HMOX1
Heme oxygenase 1
Also known as: bK286B10, HMOX1_HUMAN, HO-1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P09601
- Gene
- HMOX1
- Ensembl
- ENSG00000100292
- Chromosome
- 22
- Canonical length
- 288 aa
- Protein class
- Cancer-related genes, Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Golgi apparatus,Plasma membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
288 residues, UniProt reviewed canonical sequence.
>P09601|HMOX1
1 MERPQPDSMP QDLSEALKEA TKEVHTQAEN AEFMRNFQKG QVTRDGFKLV MASLYHIYVA
61 LEEEIERNKE SPVFAPVYFP EELHRKAALE QDLAFWYGPR WQEVIPYTPA MQRYVKRLHE
121 VGRTEPELLV AHAYTRYLGD LSGGQVLKKI AQKALDLPSS GEGLAFFTFP NIASATKFKQ
181 LYRSRMNSLE MTPAVRQRVI EEAKTAFLLN IQLFEELQEL LTHDTKDQSP SRAPGLRQRA
241 SNKVQDSAPV ETPRGKPPLN TRSQAPLLRW VLTLSFLVAT VAVGLYAMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HMOX1 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
- 1
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 740 nTPM
Expression across tissuesHPA
Tissue
- spleen: 740 nTPM
- adipose tissue: 145 nTPM
- lung: 139 nTPM
- liver: 128 nTPM
- skeletal muscle: 121 nTPM
- kidney: 116 nTPM
Single-cell type
- kupffer cells: 2,742 nCPM
- syncytiotrophoblasts: 847 nCPM
- hofbauer cells: 718 nCPM
- macrophages: 565 nCPM
- esophageal apical cells: 492 nCPM
- extravillous trophoblasts: 399 nCPM
Immune cell
- non-classical monocyte: 331 nTPM
- intermediate monocyte: 239 nTPM
- classical monocyte: 99 nTPM
- total PBMC: 71 nTPM
- neutrophil: 47 nTPM
- myeloid DC: 45 nTPM
Brain region
- thalamus: 58 nTPM
- pons: 48 nTPM
- white matter: 48 nTPM
- cerebral cortex: 43 nTPM
- medulla oblongata: 40 nTPM
- basal ganglia: 32 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about HMOX1.
Disease | AllUniProt
Conditions HMOX1 is implicated in, by any mechanism.
- Heme oxygenase 1 deficiency (HMOX1D) MIM:614034
Disease | GeneticClinVar
24 pathogenic / likely-pathogenic of 320 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Heme oxygenase 1 deficiency
- Uterine carcinosarcoma
- Malignant tumor of esophagus
- Chronic obstructive pulmonary disease
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)
- 0.93
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.52
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- angiogenesis
- cellular response to arsenic-containing substance
- cellular response to cadmium ion
- cellular response to cisplatin
- cellular response to heat
- endothelial cell proliferation
- epithelial cell apoptotic process
- erythrocyte differentiation
- erythrocyte homeostasis
- heme catabolic process
- heme oxidation
- intracellular iron ion homeostasis
- intracellular signal transduction
- low-density lipoprotein particle clearance
- macroautophagy
- multicellular organismal-level iron ion homeostasis
- negative regulation of cytokine production involved in inflammatory response
- negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
- negative regulation of ferroptosis
- negative regulation of leukocyte migration
- negative regulation of macroautophagy
- negative regulation of smooth muscle cell proliferation
- positive regulation of angiogenesis
- positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of cell migration involved in sprouting angiogenesis
- positive regulation of chemokine production
- positive regulation of epithelial cell apoptotic process
- positive regulation of macroautophagy
- positive regulation of smooth muscle cell proliferation
- regulation of angiogenesis
- regulation of transcription by RNA polymerase II
- response to hydrogen peroxide
- response to nicotine
- response to oxidative stress
- smooth muscle hyperplasia
- wound healing involved in inflammatory response
Molecular functions
- enzyme binding
- heme binding
- heme oxygenase (decyclizing) activity
- identical protein binding
- metal ion binding
- protein homodimerization activity
- structural molecule activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HMOX1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HMOX1 as an antibody target. Whether an autoantibody or antibody against HMOX1 could matter depends on whether native HMOX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HMOX1 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 HMOX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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