HMOX2

HMOX2
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2Q32, 2QPP, 2RGZ, 4WMH
Identifiers
Aliases	HMOX2, HO-2, heme oxygenase 2
External IDs	OMIM: 141251; MGI: 109373; HomoloGene: 1611; GeneCards: HMOX2; OMA:HMOX2 - orthologs
Gene location (Human)
Chr.	Chromosome 16 (human)
End	4,510,347 bp
Gene location (Mouse)
Chr.	Chromosome 16 (mouse)
End	4,584,606 bp
RNA expression pattern
	Top expressed in
	right testis; ; left testis; ; prefrontal cortex; ; left ventricle; ; apex of heart; ; superior frontal gyrus; ; Brodmann area 9; ; right auricle of heart; ; nucleus accumbens; ; body of stomach;
	Top expressed in
	spermatid; ; seminiferous tubule; ; facial motor nucleus; ; anterior horn of spinal cord; ; dentate gyrus of hippocampal formation granule cell; ; supraoptic nucleus; ; stroma of bone marrow; ; endothelial cell of lymphatic vessel; ; external carotid artery; ; internal carotid artery;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	oxidoreductase activity; protein binding; metal ion binding; heme oxygenase (decyclizing) activity; heme binding;
Cellular component	intracellular membrane-bounded organelle; endoplasmic reticulum membrane; membrane; endoplasmic reticulum; plasma membrane; specific granule membrane;
Biological process	response to hypoxia; cellular iron ion homeostasis; heme oxidation; response to oxidative stress; heme catabolic process; neutrophil degranulation; iron ion homeostasis;
	Sources:Amigo / QuickGO
Orthologs
	3163
	15369
	ENSG00000277424; ENSG00000103415
	ENSMUSG00000004070
	P30519
	O70252
NM_001127204; NM_001127205; NM_001127206; NM_001286267; NM_001286268;
	NM_001286269; NM_001286270; NM_001286271; NM_002134
	NM_001136066; NM_010443; NM_001357050; NM_001378999
NP_001120676; NP_001120677; NP_001120678; NP_001273196; NP_001273197;
	NP_001273198; NP_001273199; NP_001273200; NP_002125
	NP_001129538; NP_034573; NP_001343979; NP_001365928
	Wikidata
View/Edit Human	View/Edit Mouse

Heme oxygenase 2 is an enzyme that in humans is encoded by the HMOX2 gene.