Gene
RAB9B
RAB9B, member RAS oncogene family
- HGNC 14090↗(opens in a new tab)
- Ensembl gene ENSG00000123570↗(opens in a new tab)
- NCBI Gene 51209↗(opens in a new tab)
Summary
- Cytogenetic location
- Xq22.2
- Coordinates
- Chromosome X: 103,822,327–103,832,257 (GRCh38)
- Exons
- 3 exons across 9.9 kb
- Protein
- 201 amino acids
- Also known as
- RAB9L
- MANE Select transcript
- ENST00000243298.3NM_016370.4
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
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No Genome Test report reads RAB9B yet. The test sequences your whole genome, so your data includes it all the same.
How RAB9B is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 3.8 kb of the gene's 9.9 kb; 606 of those bases code for the protein.
Sequencing RAB9B
1
position in RAB9B 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 9.9 kb of RAB9B, introns included, not only the 3.8 kb of exons.
External links
Gene records
Transcript
Protein
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.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). RAB9B gene: RAB9B, member RAS oncogene family. Retrieved 17 October 2026, from https://dantelabs.com/genes/rab9b
Dante Labs. RAB9B gene: RAB9B, member RAS oncogene family [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rab9b
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