Traits

Traits linked to TAF11

TATA-box binding protein associated factor 11

The Human Phenotype Ontology links 18 traits to TAF11, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of head or neck

Trait	How often it is seen
Non-midline cleft of the upper lip	Often (30–79%)
Both sided cleft lip	Sometimes (5–29%)
Extra upper front tooth	Sometimes (5–29%)
Increased size of tooth	Sometimes (5–29%)
Velopharyngeal incompetence	Sometimes (5–29%)
Failure of development of between one and six teeth	Rarely (1–4%)

Abnormality of the nervous system

Trait	How often it is seen
Behavioral abnormality	Sometimes (5–29%)
Low self-esteem	Sometimes (5–29%)
Speech articulation difficulties	Sometimes (5–29%)
Specific learning disability	Rarely (1–4%)

Abnormality of the ear

Trait	How often it is seen
Chronic infections of the middle ear	Often (30–79%)
Abnormal Eustachian tube morphology	Sometimes (5–29%)
Conductive deafness	Rarely (1–4%)

Abnormality of limbs

Trait	How often it is seen
Club feet	Rarely (1–4%)

Abnormality of prenatal development or birth

Trait	How often it is seen
High levels of amniotic fluid	Rarely (1–4%)

Abnormality of the cardiovascular system

Trait	How often it is seen
All organs on wrong side of body	Rarely (1–4%)

Abnormality of the digestive system

Trait	How often it is seen
Umbilical hernia	Rarely (1–4%)

Growth abnormality

Trait	How often it is seen
Small for gestational age	Sometimes (5–29%)

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the traits linked to TAF11 and how often each is seen. Find out more at hpo.jax.org.

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