Gene
lca5
- ID
- ZDB-GENE-090313-268
- Name
- lebercilin LCA5
- Symbol
- lca5 Nomenclature History
- Previous Names
-
- si:dkey-241o6.2
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to be involved in intraciliary transport. Predicted to localize to axoneme. Human ortholog(s) of this gene implicated in Leber congenital amaurosis 5. Orthologous to human LCA5 (lebercilin LCA5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 10 figures from Qu et al., 2019
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Leber congenital amaurosis 5 | Alliance | Leber congenital amaurosis 5 | 604537 |
| Human Disease | Fish | Conditions | Citations |
|---|---|---|---|
| Leber congenital amaurosis | lca5zf3156/zf3156 | standard conditions | Qu et al., 2019 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Lebercilin domain | Lebercilin-like |
|---|---|---|---|
|
UniProtKB:A0A8M9PLA8
|
755 | ||
|
UniProtKB:A0A8M9P5L0
|
766 | ||
|
UniProtKB:A0A8M3AVL5
|
754 | ||
|
UniProtKB:E9QG33
|
754 | ||
|
UniProtKB:A0A8M9PTN2
|
753 | ||
|
UniProtKB:A0A8M6Z3Y4
|
766 | ||
|
UniProtKB:A0A8M9Q832
|
766 | ||
|
UniProtKB:A0A8M9PTM7
|
767 | ||
|
UniProtKB:A0A8M6YVF9
|
767 | ||
|
UniProtKB:A0A8M3AYN7
|
755 | ||
|
UniProtKB:A0A8M6YW27
|
753 | ||
|
UniProtKB:A0A8M9PFL3
|
766 |
Interactions and Pathways
No data available
Plasmids
No data available