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MIRAGE
TBC1 domain family member 32
Summary
- Gene Symbol
-
- TBC1D32
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Ciliopathy
- Cilium
- Cytoplasm
- Developmental protein
- Disease variant
- Holoprosencephaly
- Proteomics identification
- Reference proteome
- Retinitis pigmentosa
- Proteins
| UniProt | Protein Name |
|---|---|
| Q96NH3 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| kidney development | ||
| lens development in camera-type eye | ||
| retinal pigment epithelium development | ||
| determination of left/right symmetry | ||
| heart development |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Protein broad-minded
- Functional Category
-
- P: Inorganic ion transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| Golgi to plasma membrane protein transport |
| InterPro |
|---|
| Protein broad-minded |
| Rab-GAP-TBC domain superfamily |
