Pcnt Gene Summary [Mouse]
Predicted to enable calmodulin binding activity and molecular adaptor activity. Acts upstream of or within several processes, including embryonic organ development; mitotic spindle organization; and nervous system development. Located in several cellular components, including cis-Golgi network; intercellular bridge; and microtubule organizing center. Is expressed in several structures, including central nervous system; early conceptus; genitourinary system; respiratory system; and sensory organ. Used to study microcephalic osteodysplastic primordial dwarfism type II. Human ortholog(s) of this gene implicated in microcephalic osteodysplastic primordial dwarfism type II. Orthologous to human PCNT (pericentrin). [provided by Alliance of Genome Resources, Jul 2025]
Details
| Type | Processed Transcript |
| Official Symbol | Pcnt |
| Official Name | pericentrin (kendrin) [Source:MGI Symbol;Acc:MGI:102722] |
| Ensembl ID | ENSMUSG00000001151 |
| Bio databases IDs | |
| Aliases | pericentrin (kendrin) |
| Synonyms | C86676, KEN, Kendrin, LOC687681, m239Asp, m275Asp, MOPD2, PCN, PCNT2, PCNTB, PCTN2, pericentrin, pericentrin (kendrin), SCKL4 |
| Species | Mouse, Mus musculus |
| 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 mouse Pcnt often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Crescentin protein
- chromosome segregation protein SMC, common bacterial type
- RecF/RecN/SMC N terminal domain
- RIM-binding protein of the cytomatrix active zone
- chromosome segregation protein SMC, primarily archaeal type
- exonuclease SbcC
- Synaptonemal complex protein 1 (SCP-1)
- coiled-coil domain
- protein binding
- Calcium binding and coiled-coil domain (CALCOCO1) like
- Pericentrin-AKAP-450 domain of centrosomal targeting protein
- Laminin Domain I
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- non-insulin-dependent diabetes mellitus
- cardiovascular disorder
- microcephalic osteodysplastic primordial dwarfism, type 2
- colorectal cancer
- schizophrenia
- hereditary disorder
- Seckel syndrome
- breast carcinoma
- asthma
- microcephaly
role in cell
- migration
- proliferation
- phosphorylation in
- apoptosis
- expression in
- formation
- organization
- assembly
- misorientation
- nucleation
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
- detergent resistant lipid raft fraction
- motile cilia
- pericentriolar matrix
- cilia
- basal bodies
- centrosome
- centriole
- midbody
- cytoplasmic bridges
- asters
- microtubule organizing centers
- cytosol
- cis Golgi networks
- inner nuclear membrane
- spindle pole
- nuclear scaffolds
- centrosomal fraction
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Pcnt gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- positive regulation of intracellular protein transport
- cilium morphogenesis
- signal transduction
- mitotic spindle organization
- microtubule cytoskeleton organization
Cellular Component
Where in the cell the gene product is active
- centrosome
- centriole
- centriolar satellite
- membrane
- cytosol
- microtubule
Molecular Function
What the gene product does at the molecular level
- calmodulin binding
- protein binding
- binding, bridging