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Protein Coding Gene : Adamts13 ADAM metallopeptidase with thrombospondin type 1 motif 13

Primary Identifier  MGI:2685556 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  279028
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables endopeptidase activity. Predicted to be involved in several processes, including extracellular matrix organization; peptide catabolic process; and protein catabolic process. Predicted to act upstream of or within blood coagulation. Predicted to be located in extracellular space. Predicted to be active in extracellular matrix. Human ortholog(s) of this gene implicated in thrombotic thrombocytopenic purpura. Orthologous to human ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1 motif 13).
PHENOTYPE: Homozygous mutation of this gene results in thrombocytopenia, decreased survival, and increased susceptibility to developing thrombotic thrombocytopenic purpura after shiga toxin injection. On a different background, mutants are viable and fertile. [provided by MGI curators]
  • synonyms:
  • Adamts13,
  • ADAM metallopeptidase with thrombospondin type 1 motif 13,
  • LOC279028,
  • a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13,
  • vWF-CP mRNA for von Willebrand factor-cleaving,
  • Gm710

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

6 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For