Gene
nin
- ID
- ZDB-GENE-070725-1
- Name
- ninein (GSK3B interacting protein)
- Symbol
- nin Nomenclature History
- Previous Names
-
- si:ch211-282c13.6
- Type
- protein_coding_gene
- Location
- Chr: 13 Mapping Details/Browsers
- Description
- Predicted to have calcium ion binding activity. Involved in midbrain-hindbrain boundary development and neural tube formation. Predicted to localize to centrosome. Human ortholog(s) of this gene implicated in Seckel syndrome 7. Is expressed in anterior neural tube; brain; neuroectoderm; and posterior neural tube. Orthologous to human NIN (ninein).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from Dauber et al., 2012
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Dauber et al., 2012
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Seckel syndrome 7 | Alliance | ?Seckel syndrome 7 | 614851 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | EF-hand domain | EF-hand domain pair |
|---|---|---|---|
|
UniProtKB:A0A8M3AZC8
|
1399 | ||
|
UniProtKB:F1QE08
|
1379 |
Interactions and Pathways
No data available
Plasmids
No data available