Gene
hmox1b
- ID
- ZDB-GENE-040426-1807
- Name
- heme oxygenase 1b
- Symbol
- hmox1b Nomenclature History
- Previous Names
-
- zgc:77234 (1)
- Type
- protein_coding_gene
- Location
- Unmapped
- Description
- Predicted to enable heme oxygenase (decyclizing) activity and metal ion binding activity. Predicted to act upstream of or within heme oxidation. Is expressed in several structures, including digestive system; gill; solid lens vesicle; vein; and visual system. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); cerebrovascular disease (multiple); factor VIII deficiency; lung disease (multiple); and type 2 diabetes mellitus. Orthologous to human HMOX1 (heme oxygenase 1).
- Genome Resources
-
- Alliance (1)
- Gene:402970 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- 16 figures from 5 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:77234 (3 images)
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
chronic obstructive pulmonary disease | Alliance | {Pulmonary disease, chronic obstructive, susceptibility to} | 606963 |
Heme oxygenase-1 deficiency | 614034 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance