Gene
tctn1
- ID
- ZDB-GENE-081104-157
- Name
- tectonic family member 1
- Symbol
- tctn1 Nomenclature History
- Previous Names
-
- si:ch211-193e13.1 (1)
- Type
- protein_coding_gene
- Location
- Chr: 10 Mapping Details/Browsers
- Description
- Predicted to be involved in cilium assembly and protein localization to ciliary transition zone. Predicted to localize to MKS complex. Human ortholog(s) of this gene implicated in Joubert syndrome 13. Orthologous to human TCTN1 (tectonic family member 1).
- 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
- 1 Figure from Wang et al., 2022
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Joubert syndrome 13 | Alliance | Joubert syndrome 13 | 614173 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Tectonic | Tectonic domain |
|---|---|---|---|
|
UniProtKB:F1R392
|
534 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available