Ap4e1 Gene Summary [Rat]
Predicted to enable cargo adaptor activity. Predicted to be involved in intracellular protein transport and vesicle-mediated transport. Predicted to be located in Golgi apparatus. Predicted to be part of AP-4 adaptor complex. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 51 and stuttering. Orthologous to human AP4E1 (adaptor related protein complex 4 subunit epsilon 1). [provided by Alliance of Genome Resources, Apr 2025]
Details
| Type | Protein Coding |
| Official Symbol | Ap4e1 |
| Official Name | adaptor related protein complex 4 subunit epsilon 1 [Source:RGD Symbol;Acc:1562199] |
| Ensembl ID | ENSRNOG00000022938 |
| Bio databases IDs | |
| Aliases | adaptor related protein complex 4 subunit epsilon 1 |
| Synonyms | 2310033A20RIK, 9930028M04Rik, Adaptor protein 4 ε, adaptor related protein complex 4 subunit epsilon 1, adaptor related protein complex 4 subunit ε 1, adaptor-related protein complex AP-4, epsilon 1, adaptor-related protein complex AP-4, ε 1, AP-4 epsilon, AP-4 ε, CPSQ4, RGD1562199, SPG51, STUT1 |
| Species | Rat, Rattus norvegicus |
| Orthologies |
Protein Domains
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Ap4e1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Coatomer beta subunit appendage platform
- protein binding
- Adaptin N terminal region
Pathways
Biological processes and signaling networks where the Ap4e1 gene in rat plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- autosomal recessive nonsyndromic mental retardation
- spastic paraplegia
- AP4-deficiency syndrome
- autosomal recessive spastic paraplegia type 51
- familial persistent stuttering type 1
- developmental disorder
- congenital disorder of glycosylation type 1g
role in cell
- accumulation in
- processing in
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Cytoplasm
- endosomes
- trans Golgi network
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the rat Ap4e1 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- protein targeting
- vesicle-mediated transport
- protein localization
- intracellular protein transport
Cellular Component
Where in the cell the gene product is active
- trans-Golgi network
- endosome lumen
- AP-4 adaptor complex
- trans-Golgi network membrane
Molecular Function
What the gene product does at the molecular level
- protein binding