Gene
nup37
- ID
- ZDB-GENE-040718-363
- Name
- nucleoporin 37
- Symbol
- nup37 Nomenclature History
- Previous Names
-
- zgc:92259
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Acts upstream of or within heart development. Predicted to be part of nuclear pore outer ring. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly. Orthologous to human NUP37 (nucleoporin 37).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Haskell et al., 2017
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 3 figures from Haskell et al., 2017
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| ?Microcephaly 24, primary, autosomal recessive | 618179 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Nucleoporin Nup37 | WD40 repeat | WD40 repeat, conserved site | WD40-repeat-containing domain superfamily | WD40/YVTN repeat-like-containing domain superfamily |
|---|---|---|---|---|---|---|
|
UniProtKB:Q6DHK2
|
326 |
Interactions and Pathways
No data available
Plasmids
No data available