Gene
aimp1a
- ID
- ZDB-GENE-060825-144
- Name
- aminoacyl tRNA synthetase complex interacting multifunctional protein 1a
- Symbol
- aimp1a Nomenclature History
- Previous Names
-
- aimp1
- wu:fa95a05
- zgc:154081
- Type
- protein_coding_gene
- Location
- Chr: 1 Mapping Details/Browsers
- Description
- Predicted to enable tRNA binding activity. Is expressed in several structures, including brain; digestive system; optic cup; pectoral fin bud; and swim bladder. Human ortholog(s) of this gene implicated in hypomyelinating leukodystrophy 3. Orthologous to human AIMP1 (aminoacyl tRNA synthetase complex interacting multifunctional protein 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 7 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 1 Figure from Giong et al., 2021
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hypomyelinating leukodystrophy 3 | Alliance | Leukodystrophy, hypomyelinating, 3 | 260600 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Nucleic acid-binding, OB-fold | tRNA-binding domain | Tyrosine-tRNA ligase and regulatory protein |
|---|---|---|---|---|
|
UniProtKB:Q0P3U2
|
315 |
Interactions and Pathways
No data available
Plasmids
No data available