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
Expression
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
Phenotype
All Phenotype Data
1 Figure from Dauber et al., 2012
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With nin Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Seckel syndrome 7 Alliance ?Seckel syndrome 7 614851
Associated With nin Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR002048 EF-hand domain
Family IPR029664 Ninein
Homologous_superfamily IPR011992 EF-hand domain pair
Domain Details Per Protein
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations