LOVD ROR2 homepage

General information
Gene name receptor tyrosine kinase-like orphan receptor 2
Gene symbol ROR2
Chromosome Location 9q22
Database location
Curator Jacopo Celli
PubMed references View all (unique) PubMed references in the ROR2 database
Date of creation January 20, 2009
Last update February 21, 2012
Version ROR2 120221
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Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_008089.1
Transcript refseq ID NM_004560.3
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 31
Total number of individuals with variant(s) 228
Total number of variants reported 267
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the ROR2 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 ROR2 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the ROR2 database
Variants with no known pathogenicity Listing of all ROR2 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
Search through hidden entries Find the number of variant entries in the database (including hidden entries) matching your search terms.

Links to other resources
HGNC 10257
Entrez Gene 4920
OMIM - Gene 602337
OMIM - Disease #1 Robinow recessive syndrome (RRS)
OMIM - Disease #2 Brachydactyly type B1 (BDB1)
OMIM - Disease #3 Gastric cancer (GC)
UniProtKB (SwissProt/TrEMBL) Q01974
GeneTests ROR2
External link Orphanet

Copyright & disclaimer
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