The ROR2 gene homepage

General information
Gene symbol ROR2
Gene name receptor tyrosine kinase-like orphan receptor 2
Chromosome 9
Chromosomal band q22
Imprinted Unknown
Genomic reference NG_008089.1
Transcript reference NM_004560.3
Exon/intron information NM_004560.3 exon/intron table
Associated with diseases BDB1, ID, RRS, RRS1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (2) Juliana Mazzeu and Jacopo Celli
Total number of public variants reported 165
Unique public DNA variants reported 116
Individuals with public variants 407
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 January 20, 2009
Date last updated July 07, 2023
Version ROR2:230707

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_004560.3.
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 10257
Entrez Gene 4920
PubMed articles ROR2
OMIM - Gene 602337
OMIM - Diseases BDB1 (brachydactyly, type B1 (BDB1))
RRS1 (Robinow, autosomal recessive syndrome, type 1 (RRS1))
GeneCards ROR2
GeneTests ROR2
Orphanet ROR2

Active transcripts




NCBI ID     

NCBI Protein ID     

00018047 9 receptor tyrosine kinase-like orphan receptor 2 NM_004560.3 NP_004551.2 165

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