The ADAMTS10 gene homepage

General information
Gene symbol ADAMTS10
Gene name ADAM metallopeptidase with thrombospondin type 1 motif, 10
Chromosome 19
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NG_011840.2
Transcript reference NM_030957.2
Exon/intron information NM_030957.2 exon/intron table
Associated with diseases ID, WMS1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (2) Andreas Laner and Theresa Neuhann
Total number of public variants reported 87
Unique public DNA variants reported 62
Individuals with public variants 15
Hidden variants 8
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created July 07, 2011
Date last updated May 09, 2022
Version ADAMTS10:220509

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_030957.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL
HGNC 13201
Entrez Gene 81794
PubMed articles ADAMTS10
OMIM - Gene 608990
OMIM - Diseases WMS1 (Weill-Marchesani syndrome, type 1, recessive (WMS-1))
GeneCards ADAMTS10
GeneTests ADAMTS10
Orphanet ADAMTS10

Active transcripts




NCBI ID     

NCBI Protein ID     

00002098 19 ADAM metallopeptidase with thrombospondin type 1 motif, 10 NM_030957.2 NP_112219.2 87

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