Gene
tti2
- ID
- ZDB-GENE-110411-25
- Name
- TELO2 interacting protein 2
- Symbol
- tti2 Nomenclature History
- Previous Names
-
- si:ch73-316k5.2 (1)
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to localize to centrosome; cytosol; and nuclear lumen. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human TTI2 (TELO2 interacting protein 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
- 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 intellectual developmental disorder 39 | Alliance | Intellectual developmental disorder, autosomal recessive 39 | 615541 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Armadillo-type fold | Tti2 family |
|---|---|---|---|
|
UniProtKB:E7F592
|
488 |
Interactions and Pathways
No data available
Plasmids
No data available