NAP1L3 Gene Summary [Human]
This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010]
Details
| Type | Protein Coding |
| Official Symbol | NAP1L3 |
| Official Name | nucleosome assembly protein 1 like 3 [Source:HGNC Symbol;Acc:HGNC:7639] |
| Ensembl ID | ENSG00000186310 |
| Bio databases IDs | |
| Aliases | nucleosome assembly protein 1 like 3 |
| Synonyms | MB20, NPL3, nucleosome assembly protein 1-like 3 |
| Species | Human, Homo sapiens |
| 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 human NAP1L3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Nucleosome assembly protein (NAP)
- PTZ00007
- protein binding
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Nucleus
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human NAP1L3 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- nucleosome assembly
Cellular Component
Where in the cell the gene product is active
- nucleus
- chromatin
Molecular Function
What the gene product does at the molecular level
- protein binding
- histone binding
- chromatin binding