Gene
nup88
- ID
- ZDB-GENE-050522-297
- Name
- nucleoporin 88
- Symbol
- nup88 Nomenclature History
- Previous Names
-
- ik:tdsubc_2f7
- wu:fb16f10
- wu:fb33e09
- xx:tdsubc_2f7
- zgc:112439
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to be a structural constituent of nuclear pore. Predicted to be involved in intracellular protein transport. Predicted to localize to nuclear pore. Human ortholog(s) of this gene implicated in fetal akinesia deformation sequence syndrome 4. Is expressed in several structures, including brain; eye; immature eye; otic vesicle; and yolk syncytial layer. Orthologous to human NUP88 (nucleoporin 88).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 14 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| fetal akinesia deformation sequence syndrome 4 | Alliance | Fetal akinesia deformation sequence 4 | 618393 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Nucleoporin Nup88 | Nucleoporin NUP88/NUP82 |
|---|---|---|---|
|
UniProtKB:A0A8D3IZM5
|
|||
|
UniProtKB:A2CEI4
|
720 |
Interactions and Pathways
No data available
Plasmids
No data available