KDM6B


Lysine demethylase 6B is a protein that in humans is encoded by the KDM6B gene.

Regulation during differentiation

KDM6B was found to be expressional increased during cardiac and endothelial differentiation of murine embryonic stem cells.

Small molecule inhibition

A small molecule inhibitor has been developed to inhibit the jumonji domain of KDM6 histone demethylase family to modulate proinflammatory response in macrophages.

Role in pathology

Mutations of the KDM6B gene may cause neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities, which was first described in 2019 by Stolerman et al.
Standard laboratory exome sequencing can be used to identify the KDM6B gene variant.

Clinical picture

A 2019 study on symptoms from KDM6B variations reported:
A further 2023 international study
reported on the following clinical features among individuals with pathogenic KDM6B variants:
Feature Namep valueTotal %
Males0.5073%
Increased birth weight 0.3317%
Increased weight 0.5914%
Tall stature 1.08%
Macrocephaly 1.026%
At least one feature of overgrowth syndrome1.030%
Language/speech delay0.1594%
Motor delay1.089%
Intellectual disability0.1463%
Autism spectrum 0.5161%
Behavior problems, non-ASD0.7060%
Psychotic disorders 1.020%
Seizures0.5813%
Sleep disturbances0.0932%
Movement disorder/gait disturbances/hypertonia/ataxia0.6724%
Hypotonia1.057%
Neonatal feeding difficulties or gastroesophageal reflux1.051%
Constipation1.018%
Congenital heart disease0.5813%
Cleft lip/palate/uvula0.03b4%
Genitourinary system abnormalities1.010%
Joint hypermobility1.042%
Scoliosis/kyphosis/lordosis0.5813%
Syndactyly0.159%
Short fingers or toes1.09%
Broad fingers/fingertips/hands/toes/feet1.020%
Myopia/amblyopia0.0833%
Strabismus0.5813%
Hearing loss1.02%
Recurrent ear infections1.012%

Epidemiology

For patients reporting intellectual disability and/or developmental delay, approximately 0.12% have de novo alterations in the KDM6B gene.

Related conditions

Overlapping phenotypic features for patients between KDM6A associated with Kabuki syndrome and KDM6B variations include prominent ears, abnormal dentition, congenital heart disease, feeding difficulties, cryptorchidism, joint hyper-mobility, developmental delay, hypotonia, and behavioral difficulties.

Ongoing research

According to a study published in 2022, pathologic mutations of KDM6B were found in five patients with cerebral folate deficiency.