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Symbol
Name
ID
Kmt2d
lysine (K)-specific methyltransferase 2D
MGI:2682319
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Feeding difficulties in infancy
Atypical behavior
Weak cry
Disease(s) Associated with KMT2D
Kabuki syndrome

Mouse Phenotypes
impaired contextual conditioning behavior
abnormal object recognition memory
impaired spatial learning
decreased coping response
increased grooming behavior
abnormal motor capabilities/coordination/movement
abnormal pinna reflex
impaired righting response
hyporesponsive to tactile stimuli
limb grasping
impaired coordination
abnormal gait
short stride length
increased vertical activity
increased locomotor activity
Availability Mouse Genotype
Kmt2dbapa/Kmt2dbapa
Kmt2dGt(RRT024)Byg/Kmt2d+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory