PKHD1L1 Gene Summary [Human]
Predicted to act upstream of or within sensory perception of sound. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]
Details
| Type | Protein Coding |
| Official Symbol | PKHD1L1 |
| Official Name | PKHD1 like 1 [Source:HGNC Symbol;Acc:HGNC:20313] |
| Ensembl ID | ENSG00000205038 |
| Bio databases IDs | |
| Aliases | PKHD1 like 1 |
| Synonyms | Ay219182, DFNB124, F430003O07Rik, PKHD1 like 1, PKHDL1, polycystic kidney and hepatic disease 1-like 1 |
| 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 PKHD1L1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Right handed beta helix region
- G8 domain
- Cupredoxin superfamily
- IPT
- PA14 domain
- IPT/TIG domain
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.
- Extracellular Space
- cytosol
- stereocilia
- glycocalyx
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human PKHD1L1 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- sensory perception of sound
- immune response
Cellular Component
Where in the cell the gene product is active
- extracellular space
- membrane
- cytosol
- stereocilium bundle tip
Molecular Function
What the gene product does at the molecular level
- signaling receptor activity