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Gene

ROR2

ROR family WNT receptor 2

Summary

Cytogenetic location
9q22.31
Coordinates
Chromosome 9: 91,722,601–91,950,228 (GRCh38)
Exons
9 exons across 227.6 kb
Protein
943 amino acids
Previous symbols
NTRKR2, BDB, BDB1
MANE Select transcript
ENST00000375708.4NM_004560.4
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads ROR2 yet. The test sequences your whole genome, so your data includes it all the same.

How ROR2 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 9, with a bracket where ROR2 sits. ROR2 and 6 genes near it on chromosome 9, from 91,336,415 to 92,336,414.Chromosome 99q22.31p24.3p24.2p24.1p23p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q13q21.11q21.12q21.13q21.2q21.31q21.32q21.33q22.1q22.2q22.31q22.32q22.33q31.1q31.2q31.3q32q33.1q33.2q33.3q34.11q34.12q34.13q34.2q34.391.4 Mb91.6 Mb91.8 Mb92 Mb92.2 MbAUH: 91,213,805–91,361,972, reverse strandAUHNFIL3: 91,408,371–91,483,593, reverse strandNFIL3ROR2: 91,722,601–91,950,228, reverse strandROR2SPTLC1: 92,000,087–92,115,491, reverse strandSPTLC1IARS1: 92,210,199–92,293,854, reverse strandIARS1NOL8: 92,297,358–92,325,636, reverse strandNOL8CENPP: 92,325,625–92,620,529, forward strandCENPPDiagram of ROR2: 9 exons on the reverse strand of chromosome 9Exon 9: 10 known disease-causing sitesExon 8: 3 known disease-causing sitesExon 7: 4 known disease-causing sitesExon 6: 3 known disease-causing sitesExon 5: 1 known disease-causing siteExon 3: 1 known disease-causing siteExon 9: 91,722,601–91,725,107, 2,507 basesExon 8: 91,726,541–91,726,743, 203 basesExon 7: 91,730,910–91,731,155, 246 basesExon 6: 91,733,122–91,733,436, 315 basesExon 5: 91,737,391–91,737,518, 128 basesExon 4: 91,756,071–91,756,101, 31 basesExon 3: 91,757,272–91,757,559, 288 basesExon 2: 91,775,741–91,775,818, 78 basesExon 1: 91,949,867–91,950,228, 362 bases9515′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 4.2 kb of the gene's 227.6 kb; 2,832 of those bases code for the protein.

How a genome test reads ROR2

25

positions in ROR2 where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 227.6 kb of ROR2, introns included, not only the 4.2 kb of exons.

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). ROR2 gene: ROR family WNT receptor 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/ror2

Vancouver

Dante Labs. ROR2 gene: ROR family WNT receptor 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/ror2

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