LOVD ANKH homepage

General information
Gene name Ankylosis, progressive homolog (mouse)
Gene symbol ANKH
Chromosome Location 5p15.2
Database location http://grenada.lumc.nl/LOVD2/shared1
Curator LOVD-team, but with Curator vacancy and Jirko Kühnisch
PubMed references View all (unique) PubMed references in the ANKH database
Date of creation April 29, 2010
Last update February 03, 2012
Version ANKH120203
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file coding DNA reference sequence for describing sequence variants
Genomic refseq ID NG_008273.1
Transcript refseq ID NM_054027.4
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 1
Total number of individuals with variant(s) 17
Total number of variants reported 20
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NOTE The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nº 200754 - the GEN2PHEN project.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the ANKH database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the ANKH database, without patient data
Complete sequence variant listing Listing of all sequence variants in the ANKH database
Variants with no known pathogenicity Listing of all ANKH variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
Homepage http://www.LOVD.nl/ANKH
HGNC 15492
Entrez Gene 56172
OMIM - Gene 605145
OMIM - Disease #1 chondrocalcinosis, type 2 (CCAL-2)
OMIM - Disease #2 craniometaphyseal dysplasia, autosomal dominant (CMDD)
UniProtKB (SwissProt/TrEMBL) Q9HCJ1
HGMD ANKH
GeneCards ANKH
GeneTests ANKH
External link Orphanet

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2016. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.