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MIRAGE
tectonic family member 2
Summary
- Gene Symbol
-
- TCTN2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cell projection
- Cilium biogenesis/degradation
- Cytoskeleton
- Glycoprotein
- Joubert syndrome
- Meckel syndrome
- Proteomics identification
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q96GX1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| smoothened signaling pathway | ||
| smoothened signaling pathway | ||
| cilium assembly | ||
| cilium assembly | ||
| protein localization to ciliary transition zone |
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm | ||
| cytoskeleton | ||
| MKS complex | ||
| MKS complex | ||
| ciliary membrane |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- tectonic-2
- Functional Category
-
- G: Carbohydrate transport and metabolism
- L: Replication, recombination and repair
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| cell projection organization |
| protein localization to ciliary transition zone |
| smoothened signaling pathway |
| InterPro |
|---|
| Tectonic domain |
| Tectonic |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070122 | Meckel syndrome 8 | |
| DOID:0110993 | Joubert syndrome 24 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 67978 | Xenbase:XB-GENE-1015381 | MOUSE47064 | |
| 79867 | Xenbase:XB-GENE-1015381 | ||
| 477445 | CANLF10245 | ||
| 689779 | Xenbase:XB-GENE-1015381 | ||
| 721415 | MACMU03860 | ||
| 100153315 | PIGXX06697 | ||
| 100454231 | PONAB06552 | ||
| 100615573 | PANTR07216 | ||
| 100630826 | HORSE41069 | ||
| 100662238 | LOXAF03839 |
