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MIRAGE
tectonic family member 1
Summary
- Gene Symbol
-
- TCTN1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cell projection
- Cilium biogenesis/degradation
- Cytoskeleton
- Developmental protein
- Glycoprotein
- Joubert syndrome
- Proteomics identification
- Reference proteome
- Secreted
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| B4DIB9 |
|
| A0A087X1J4 |
|
| A8MW34 |
|
| Q05BR9 |
|
| Q2MV58 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| in utero embryonic development | ||
| neural tube formation | ||
| regulation of smoothened signaling pathway | ||
| somatic motor neuron differentiation | ||
| telencephalon development |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular space | ||
| cytosol | ||
| cytoskeleton | ||
| membrane | ||
| MKS complex |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- tectonic-1
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| cell projection organization |
| protein localization to ciliary transition zone |
| InterPro |
|---|
| Tectonic domain |
| Tectonic |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110982 | Joubert syndrome 13 |
