HSDL1 Gene Summary [Human]
Predicted to enable oxidoreductase activity. Located in intermediate filament cytoskeleton and mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | HSDL1 |
| Official Name | hydroxysteroid dehydrogenase like 1 [Source:HGNC Symbol;Acc:HGNC:16475] |
| Ensembl ID | ENSG00000103160 |
| Bio databases IDs | |
| Aliases | hydroxysteroid dehydrogenase like 1, short chain dehydrogenase/reductase family 12C, member 3 |
| Synonyms | 2700067E09Rik, hydroxysteroid dehydrogenase like 1, RGD1308433, SDR12C3 |
| 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 HSDL1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Rossmann-fold NAD(P)(+)-binding proteins
- enzyme
- protein binding
- short chain dehydrogenase
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.
- Cytoplasm
- intermediate filament cytoskeleton
- intracellular membrane-bounded organelle
- Mitochondria
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human HSDL1 gene, providing context for its role in the cell.
Cellular Component
Where in the cell the gene product is active
- intermediate filament cytoskeleton
- intracellular membrane-bounded organelle
- mitochondrion
Molecular Function
What the gene product does at the molecular level
- steroid dehydrogenase activity
- protein binding