LOVD COLEC11 homepage

General information
Gene name collectin sub-family member 11
Gene symbol COLEC11
Chromosome Location 2p25.3
Database location http://grenada.lumc.nl/LOVD2/shared1
Curator LOVD-team, but with Curator vacancy
PubMed references View all (unique) PubMed references in the COLEC11 database
Date of creation June 16, 2011
Last update June 30, 2011
Version COLEC11 110630
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file Genomic reference sequence for describing sequence variants
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 4
Total number of individuals with variant(s) 7
Total number of variants reported 14
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the COLEC11 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 COLEC11 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the COLEC11 database
Variants with no known pathogenicity Listing of all COLEC11 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
HGNC 17213
Entrez Gene 78989
OMIM - Gene 612502
UniProtKB (SwissProt/TrEMBL) Q9BWP8
External link Orphanet