Gene
ANKRD11
ankyrin repeat domain 11
- HGNC 21316↗(opens in a new tab)
- Ensembl gene ENSG00000167522↗(opens in a new tab)
- NCBI Gene 29123↗(opens in a new tab)
Summary
- Cytogenetic location
- 16q24.3
- Coordinates
- Chromosome 16: 89,267,630–89,490,561 (GRCh38)
- Exons
- 13 exons across 222.9 kb
- Protein
- 2,663 amino acids
- Also known as
- LZ16, T13, ANCO1, ANCO-1
- MANE Select transcript
- ENST00000301030.10NM_013275.6
- 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 ANKRD11, 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
Intellectual Disability
One of 233 genes linked to it
- ClinGen rates the link definitive
- 6 GenCC submitters rate it definitive or strong
How ANKRD11 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 9.3 kb of the gene's 222.9 kb; 7,992 of those bases code for the protein.
How a genome test reads ANKRD11
421
positions in ANKRD11 where ClinVar classes a change as pathogenic or likely pathogenic
101 of them (24%) fall in regions short reads find hard.
- Low mappability (35 sites)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
- Segmental duplications (66 sites)Copies of at least 1 kb sharing at least 90% identity with another part of the genome (paralogues, pseudogenes); reads may align to the wrong copy.
A whole genome covers all 222.9 kb of ANKRD11, introns included, not only the 9.3 kb of exons.
Genes linked to the same conditions
- ACSL4acyl-CoA synthetase long chain family member 4Shares 1 condition
- ADKadenosine kinaseShares 1 condition
- ADNPactivity dependent neuroprotector homeoboxShares 1 condition
- AFF2ALF transcription elongation factor 2Shares 1 condition
- AHDC1AT-hook DNA binding motif containing 1Shares 1 condition
- ALKBH8alkB homolog 8, tRNA methyltransferaseShares 1 condition
- ANK3ankyrin 3Shares 1 condition
- AP1S2adaptor related protein complex 1 subunit sigma 2Shares 1 condition
- AP2M1adaptor related protein complex 2 subunit mu 1Shares 1 condition
- ARHGEF9Cdc42 guanine nucleotide exchange factor 9Shares 1 condition
- ARID1AAT-rich interaction domain 1AShares 1 condition
- ARID1BAT-rich interaction domain 1BShares 1 condition
Traits linked to ANKRD11
The Human Phenotype Ontology lists these as features of the rare conditions ANKRD11 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Increased size of tooth
- Long philtrum
- Nasal tip, upturned
- Triangular face
- Broad opening between the eyelids
- High forehead
- Low frontal hairline
- Low hairline at back of neck
Show 31 more traits
- Abnormally small head
- Broad head shape
- Central incisor gap
- Cleft palate
- Corners of eye widely separated
- Failure of development of more than six teeth
- Frontal bossing
- High palate
- Little lower jaw
- Monobrow
- Pointed chin
- Prominent nasal bridge
- Short neck
- Smooth philtrum
- Thick eyebrow
- Thin red part of the upper lip
- Underdeveloped tissue around nostril
- Webbed neck
- Wide mouth
- Decreased width of the skull
- Downward slanting of the opening between the eyelids
- Full lips
- Highly arched eyebrow
- Increased nuchal translucency
- Long face
- Only one upper front tooth
- Persistent open anterior fontanelle
- Round face
- Skin tag in front of the ear
- Tented mouth
- Upward slanting of the opening between the eyelids
Abnormality of the musculoskeletal system
- Delayed bone maturation
- Abnormally shaped skeletal
- Cervical ribs
- Scoliosis
- Thoracic kyphosis
- Vertebral fusion
- Abnormal formation of the hip
- Hunched back
Show 2 more traits
Abnormality of limbs
- Curvature of little finger
- Short palm
- Curvature of finger
- Cutaneous syndactyly
- Single transverse palmar crease
- Attachment of thumb close to wrist
- Ulnar deviation of the 2nd finger
- Radial deviation of finger
Show 1 more trait
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.
- 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
Dante Labs. (n.d.). ANKRD11 gene: ankyrin repeat domain 11. Retrieved 17 October 2026, from https://dantelabs.com/genes/ankrd11
Dante Labs. ANKRD11 gene: ankyrin repeat domain 11 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/ankrd11
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks