Gene
loxhd1b
- ID
- ZDB-GENE-081104-370
- Name
- lipoxygenase homology PLAT domains 1b
- Symbol
- loxhd1b Nomenclature History
- Previous Names
-
- si:dkey-210e6.2
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to have catalase activity and heme binding activity. Predicted to be involved in oxidation-reduction process. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy; autosomal recessive nonsyndromic deafness 77; and orofacial cleft. Orthologous to human LOXHD1 (lipoxygenase homology domains 1).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 2 figures from Shi et al., 2023
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
autosomal recessive nonsyndromic deafness 77 | Alliance | Deafness, autosomal recessive 77 | 613079 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Inner ear hair cell lipoxygenase homology domain-containing protein | PLAT/LH2 domain | PLAT/LH2 domain superfamily |
---|---|---|---|---|
UniProtKB:A0A8M1QHF7
|
2268 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
loxhd1b-201
(1)
|
Ensembl | 6,884 nt | ||
mRNA |
loxhd1b-202
(1)
|
Ensembl | 6,060 nt |
Interactions and Pathways
No data available
Plasmids
No data available