Gene
HOXA11
homeobox A11
- HGNC 5101↗(opens in a new tab)
- Ensembl gene ENSG00000005073↗(opens in a new tab)
- NCBI Gene 3207↗(opens in a new tab)
Summary
- Cytogenetic location
- 7p15.2
- Coordinates
- Chromosome 7: 27,181,157–27,185,232 (GRCh38)
- Exons
- 2 exons across 4.1 kb
- Protein
- 313 amino acids
- Previous symbols
- HOX1I, HOX1
- MANE Select transcript
- ENST00000006015.4NM_005523.6
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read HOXA11, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Inherited Thrombocytopenias
- Inherited Thrombocytopenia
A group of conditions causing a lifelong low platelet count, linked to genes such as MYH9, ANKRD26, ETV6, WAS, MPL, RBM8A, GATA1 and MECOM, and inherited in dominant, recessive or X-linked patterns.
- 1 GenCC submitter rates it definitive or strong
What knowing changes
A genetic diagnosis avoids misdiagnosis as immune thrombocytopenia, with unnecessary steroids or spleen removal, and guides monitoring for related kidney, hearing or blood problems.
How HOXA11 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 2.7 kb of the gene's 4.1 kb; 942 of those bases code for the protein.
Genes linked to the same conditions
- ACTBactin betaShares 1 condition
- ACTN1actinin alpha 1Shares 1 condition
- ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13Shares 1 condition
- ANKRD26ankyrin repeat domain 26Shares 1 condition
- ARPC1Bactin related protein 2/3 complex subunit 1BShares 1 condition
- CDC42cell division cycle 42Shares 1 condition
- CYCScytochrome c, somaticShares 1 condition
- DIAPH1diaphanous related formin 1Shares 1 condition
- ETV6ETS variant transcription factor 6Shares 1 condition
- FLI1Fli-1 proto-oncogene, ETS transcription factorShares 1 condition
- FYB1FYN binding protein 1Shares 1 condition
- GALEUDP-galactose-4-epimeraseShares 1 condition
Traits linked to HOXA11
The Human Phenotype Ontology lists these as features of the rare conditions HOXA11 can cause. Each trait's page lists the other genes linked to it.
Abnormality of limbs
- Curvature of little finger
- Fused forearm bones
- Finger syndactyly
- Bowing of outer large bone of the forearm
- Curving of inner forearm bone
- Hip dislocation
- Limited pronation/supination of forearm
- Proximal radio-ulnar synostosis
Show 2 more traits
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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- 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
Dante Labs. (n.d.). HOXA11 gene: homeobox A11. Retrieved 17 October 2026, from https://dantelabs.com/genes/hoxa11
Dante Labs. HOXA11 gene: homeobox A11 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/hoxa11
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks