Mus musculus Gene: Adamts10
Summary
InnateDB Gene IDBG-167113.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Adamts10
Gene Name a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000024299
Encoded Proteins
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000142303:
This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:33524204-33553782
Strand Forward strand
Band B1
Transcripts
ENSMUST00000087623 ENSMUSP00000084905
ENSMUST00000173931 ENSMUSP00000133434
ENSMUST00000173241 ENSMUSP00000134298
ENSMUST00000174170
ENSMUST00000173030 ENSMUSP00000134549
ENSMUST00000173013 ENSMUSP00000134181
ENSMUST00000172922 ENSMUSP00000133891
ENSMUST00000174348 ENSMUSP00000133856
ENSMUST00000173813
ENSMUST00000174104
ENSMUST00000173972
ENSMUST00000174666
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004222 metalloendopeptidase activity
GO:0005515 protein binding
GO:0008233 peptidase activity
GO:0008270 zinc ion binding
Biological Process
GO:0006508 proteolysis
Cellular Component
GO:0001527 microfibril
GO:0031012 extracellular matrix
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Post-translational protein modification pathway
O-linked glycosylation pathway
Metabolism of proteins pathway
O-glycosylation of TSR domain-containing proteins pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL G3UZ08
UniProt Splice Variant
Entrez Gene 224697
UniGene Mm.29304
RefSeq NM_172619 XM_006524100 XM_006524101 XM_006524102 XM_006524103 XM_006524104 XM_006524105 XM_006524106
OMIM
CCDS CCDS37566
HPRD
IMGT
MGI ID MGI:2449112
MGI Symbol Adamts10
EMBL CH466660 CT030734
GenPept EDL10193 EDL10195
RNA Seq Atlas 224697