Gene
RAB11B
RAB11B, member RAS oncogene family
- HGNC 9761↗(opens in a new tab)
- Ensembl gene ENSG00000185236↗(opens in a new tab)
- NCBI Gene 9230↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.2
- Coordinates
- Chromosome 19: 8,390,360–8,404,434 (GRCh38)
- Exons
- 5 exons across 14.1 kb
- Protein
- 218 amino acids
- Also known as
- H-YPT3
- MANE Select transcript
- ENST00000328024.11NM_004218.4
- 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.
library(jsonlite)
url <- "https://dantelabs.com/genes/rab11b.json"
page <- fromJSON(url)
page$gene$nameRead RAB11B, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads RAB11B yet. The test sequences your whole genome, so your data includes it all the same.
How RAB11B is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
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 1.6 kb of the gene's 14.1 kb; 657 of those bases code for the protein.
Sequencing RAB11B
8Low
How hard RAB11B is to sequence with short reads, out of 100Each bar is the share of RAB11B's exon bases in that kind of difficult region. The score weighs them by how much each costs a short-read call: 0 when no base is in any, 100 when every base is in all of them.
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 30%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 15%.6.7%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.74%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
3
positions in RAB11B 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 14.1 kb of RAB11B, introns included, not only the 1.6 kb of exons.
Traits linked to RAB11B
The Human Phenotype Ontology lists these as features of the rare conditions RAB11B can cause. Each trait's page lists the other genes linked to it.
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.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). RAB11B gene: RAB11B, member RAS oncogene family. Retrieved 17 October 2026, from https://dantelabs.com/genes/rab11b
Dante Labs. RAB11B gene: RAB11B, member RAS oncogene family [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rab11b
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks