Gene
tctn2
- ID
- ZDB-GENE-030131-751
- Name
- tectonic family member 2
- Symbol
- tctn2 Nomenclature History
- Previous Names
-
- fb44f11
- si:ch211-89f7.3
- wu:fb44f11
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Involved in determination of left/right symmetry. Predicted to localize to MKS complex. Human ortholog(s) of this gene implicated in Joubert syndrome 24 and Meckel syndrome 8. Orthologous to human TCTN2 (tectonic family member 2).
- 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
- 2 figures from Liu et al., 2018
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Joubert syndrome 24 | Alliance | Joubert syndrome 24 | 616654 |
Meckel syndrome 8 | Alliance | ?Meckel syndrome 8 | 613885 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Tectonic | Tectonic domain |
---|---|---|---|
UniProtKB:F1R5E2
|
702 |
Interactions and Pathways
No data available
Plasmids
No data available