JAG2 Gene Summary [Human]
The Notch signaling pathway is an intercellular signaling mechanism that is essential for proper embryonic development. Members of the Notch gene family encode transmembrane receptors that are critical for various cell fate decisions. The protein encoded by this gene is one of several ligands that activate Notch and related receptors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Details
| Type | Protein Coding |
| Official Symbol | JAG2 |
| Official Name | jagged canonical Notch ligand 2 [Source:HGNC Symbol;Acc:HGNC:6189] |
| Ensembl ID | ENSG00000184916 |
| Bio databases IDs | |
| Aliases | jagged canonical Notch ligand 2 |
| Synonyms | D12Ggc2e, HJ2, JAGGED 2, jagged canonical Notch ligand 2, LGMDR27, mJagged2-1, SER2, Serh, Serrate2, sm |
| 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 JAG2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- extracellular domain
- von Willebrand factor type C domain
- N terminus of Notch ligand C2-like domain
- Human growth factor-like EGF
- protein binding
- growth factor
- EGF repeat
- notch binding
- Delta serrate ligand
- EGF_CA
Pathways
Biological processes and signaling networks where the JAG2 gene in human 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
- neoplasia
- organismal death
- cyanosis
- tinnitus
- autosomal recessive limb-girdle muscular dystrophy type 27
- cleft palate
- syndactyly
- serous ovarian cancer
- primary biliary cirrhosis
- limb-girdle muscular dystrophy type 2
role in cell
- expression in
- number
- quantity
- differentiation
- proliferation
- survival
- apoptosis
- development
- orientation
- abnormal morphology
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
- Cytoplasm
- cell surface
- perinuclear region
- cellular membrane
- Nucleus
- Plasma Membrane
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the human JAG2 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- spermatogenesis
- odontogenesis of dentin-containing tooth
- auditory receptor cell fate commitment
- positive regulation of Notch signaling pathway
- regulation of cell proliferation
- respiratory system process
- T cell differentiation
- thymic T cell selection
- skeletal system development
- Notch signaling pathway
- in utero embryonic development
- gamma-delta T cell differentiation
- cell differentiation
- morphogenesis of embryonic epithelium
- regulation of cell adhesion
Cellular Component
Where in the cell the gene product is active
- plasma membrane
Molecular Function
What the gene product does at the molecular level
- growth factor activity
- protein binding
- calcium ion binding
- Notch binding