Gene
lhfpl5a
- ID
- ZDB-GENE-110131-8
- Name
- LHFPL tetraspan subfamily member 5a
- Symbol
- lhfpl5a Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 11 Mapping Details/Browsers
- Description
- Involved in detection of mechanical stimulus involved in sensory perception and protein localization to cilium. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 67. Orthologous to human LHFPL5 (LHFPL tetraspan subfamily member 5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Erickson et al., 2020
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal recessive nonsyndromic deafness 67 | Alliance | Deafness, autosomal recessive 67 | 610265 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019372 | Lipoma HMGIC fusion partner-like protein |
Domain Details Per Protein
| Protein | Length | Lipoma HMGIC fusion partner-like protein |
|---|---|---|
|
UniProtKB:F1Q837
|
219 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
lhfpl5a-201
(1)
|
Ensembl | 1,137 nt | ||
| mRNA |
lhfpl5a-202
(1)
|
Ensembl | 1,051 nt |
Interactions and Pathways
No data available
Plasmids
No data available