ADAMTS19 Gene Summary [Human]

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene has high sequence similarity to the protein encoded by ADAMTS16, another family member. [provided by RefSeq, Jul 2008]

Details

Type
Nonsense Mediated Decay
Official Symbol
ADAMTS19
Official Name
ADAM metallopeptidase with thrombospondin type 1 motif 19 [Source:HGNC Symbol;Acc:HGNC:17111]
Ensembl ID
ENSG00000145808
Bio databases IDs NCBI: 171019 Ensembl: ENSG00000145808
Aliases ADAM metallopeptidase with thrombospondin type 1 motif 19
Synonyms 4831407I23Rik, ADAM metallopeptidase with thrombospondin type 1 motif 19, ADAM metallopeptidase with thrombospondin type 1 motif, 19, CVDP2, D230034E10RIK
Species
Human, Homo sapiens
OrthologiesMouseRat

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 ADAMTS19 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Thrombospondin type 1 repeats
  • Reprolysin family propeptide
  • Thrombospondin type 1 domain
  • ADAM-TS Spacer 1
  • ZnMc
  • Metallo-peptidase family M12B Reprolysin-like
  • ADAMTS cysteine-rich domain 2
  • peptidase
  • Reprolysin (M12B) family zinc metalloprotease
  • Spondin-like TSP1 domain

Pathways

Biological processes and signaling networks where the ADAMTS19 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
  • osteoarthritis
  • cardiac valvular dysplasia type 2
  • idiopathic scoliosis
  • major depression
  • congenital heart disease
  • acute myeloid leukemia
  • open-angle glaucoma
  • sexual disorder
  • Dupuytren contracture
  • diabetic nephropathy
regulated by
role in cell
  • organization

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
  • extracellular matrix

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human ADAMTS19 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • aortic valve morphogenesis
  • mitral valve morphogenesis
  • proteolysis
  • pulmonary valve morphogenesis
  • extracellular matrix organization
  • tricuspid valve morphogenesis
  • collagen fibril organization
  • ventricular septum morphogenesis

Cellular Component

Where in the cell the gene product is active
  • extracellular matrix
  • extracellular region

Molecular Function

What the gene product does at the molecular level
  • metal ion binding
  • metalloendopeptidase activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.